Protocol summary
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Study aim
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Comparison of clinical and immunological effectiveness of laser acupuncture versus manual acupuncture and routine drug treatment in patients with knee osteoarthritis referred to the rheumatology clinic of Ghaem Hospital
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Design
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This is a Phase 2, randomized, single-blind, parallel-group, controlled clinical trial involving 90 patients. Randomization will be performed using blocks of six, with the allocation sequence generated via the Sealed Envelope website. The process involves 16 blocks of six—each containing two instances of letters A, B, and C—assigned to numbers 1 through 90. The letters will be placed inside opaque envelopes corresponding to these numbers; the envelope will be sealed with the number written on the outside. Participants will select envelopes sequentially, starting with number 1, and will be assigned to the corresponding group upon opening the envelope, thereby ensuring equal distribution across the three groups.
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Settings and conduct
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After reviewing the inclusion criteria and filling out the informed consent form, patients are referred by a rheumatologist from the Rheumatology Clinic of Ghaem Hospital to the Acupuncture Clinic of Imam Reza Hospital in Mashhad and are randomly assigned to one of the three study groups. Blinding is fully described in the relevant section.
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Participants/Inclusion and exclusion criteria
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Patients 45 years and older
Having the diagnostic criteria of the American College of Rheumatology
Complaint of knee pain for more than 3 months
Last 6 months radiology: Grade 2 or 3 Kellogg Lawrence
Medial tibiofemoral osteoarthritis more than lateral in at least one knee
NSR 4 or more
Not taking omega-3 and glucosamine during the study
Not having undergone physical therapy in the past three months
No other concomitant rheumatic disease
Willingness to sign informed consent
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Intervention groups
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Manual acupuncture, laser acupuncture, laser sham control
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Main outcome variables
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Pain, knee joint function and stiffness, blood levels of immunological factors, quality of life, need for painkillers
General information
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Reason for update
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Acronym
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IRCT registration information
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IRCT registration number:
IRCT20110809007265N15
Registration date:
2025-11-01, 1404/08/10
Registration timing:
prospective
Last update:
2026-09-14, 1405/06/23
Update count:
1
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Registration date
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2025-11-01, 1404/08/10
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Registrant information
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Recruitment status
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recruiting
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Funding source
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Expected recruitment start date
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2025-12-22, 1404/10/01
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Expected recruitment end date
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2027-03-21, 1406/01/01
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Actual recruitment start date
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empty
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Actual recruitment end date
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empty
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Trial completion date
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empty
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Scientific title
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Comparison of the clinical and immunological effectiveness of laser acupuncture, manual acupuncture, and sham in the treatment of knee osteoarthritis
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Public title
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Comparison of laser and manual acupuncture in knee osteoarthritis
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Purpose
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Treatment
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Inclusion/Exclusion criteria
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Inclusion criteria:
Patients aged 45 and above
Patients with the diagnostic criteria of the American College of Rheumatology
Complaint of knee pain for more than 3 months
Radiological examination in the last 6 months indicating grade 2 or 3 of Kellgren lawrence with interpretation and confirmation by a respected rheumatologist
Patients with medial tibiofemoral osteoarthritis in at least one knee
A score of 4 or higher on the NSR
Do not consume omega-3 and glucosamine while studying
Not undergoing physiotherapy in the past three months
At the same time, they should not have another rheumatic disease such as rheumatoid arthritis
Exclusion criteria:
Previous knee surgery on the knee being evaluated or pending any surgery for both knees
Knee pain caused by other pathologies (such as meniscus tear, rheumatoid arthritis, joint space infection, malignancy, gout, lumbosacral diseases with lower limb symptoms, etc.)
A history of arthroscopy within the last year or a history of intra-articular injection within the last 6 months for knee evaluation
Each of the knees has received acupuncture/physical therapy in the past 6 months
Severe acute or chronic organic or neuropsychiatric disorder
Coagulation disorders (such as hemophilia)
Autoimmune disorders
Malignancies
Patients with epilepsy or those with a pacemaker
Drug use
Physiotherapy a month ago
Preparation for pregnancy, pregnancy or breastfeeding period
Patients who have participated in other acupuncture clinical studies in the past month
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Age
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From 45 years old
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Gender
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Both
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Phase
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3
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Groups that have been masked
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- Participant
- Care provider
- Outcome assessor
- Data analyser
- Data and Safety Monitoring Board
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Sample size
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Target sample size:
90
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Randomization (investigator's opinion)
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Randomized
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Randomization description
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In the random allocation, we will use blocks of 6 and use the sealedenvelope website. In this type of allocation, 16 blocks of 6 are generated by the system (2 of each letter) and are numbered from 1 to 90. The letters are placed in the order of their numbers in a matte envelope, the number is written on the envelope, and the lid is closed. People start taking the envelope in the order of their arrival from envelope number 1, open it, and are referred to the relevant group. In this way, people are placed equally in three groups. After the blocks are determined, they are placed in envelopes that cannot be seen from the outside, the letters are placed in them, and a number is written in order. People take the envelope in the order of their arrival and are assigned to the relevant group.
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Blinding (investigator's opinion)
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Single blinded
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Blinding description
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All patients who enter the study first fill out an informed consent form, which states that the patient will be randomly assigned to one of three study groups: manual acupuncture, laser acupuncture, and the control group. Given that sham laser acupuncture is performed in the control group, patients in the laser acupuncture and control groups will be blinded to receiving the laser acupuncture intervention but will be aware that they will not receive conventional acupuncture. Patients in the manual acupuncture group will also likely notice the difference between this method and laser acupuncture, so blinding can only be done partially for the laser acupuncture and sham laser acupuncture groups. Blinding of the acupuncture specialist (principal investigator) is not possible. The referring rheumatologist, the nurse who takes the blood sample, the immunologist and expert, and the statistician will be responsible for collecting data and evaluating the outcomes for the assigned group of patients. The acupuncture resident responsible for data collection and overall patient follow-up will also be blinded to the assigned patient group.
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Placebo
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Used
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Assignment
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Parallel
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Other design features
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Ethics committees
1
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Ethics committee
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Approval date
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2025-06-21, 1404/03/31
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Ethics committee reference number
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IR.MUMS.REC.1404.154
Health conditions studied
1
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Description of health condition studied
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Gonarthrosis [arthrosis of knee]
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ICD-10 code
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M17
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ICD-10 code description
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Osteoarthritis of knee
Primary outcomes
1
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Description
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Pain
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Timepoint
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The trial duration is 16 weeks, including 8 weeks of treatment and 8 weeks of follow-up.
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Method of measurement
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Pain based on Visual Analogue Scale
2
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Description
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Knee joint performance status
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Timepoint
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Before treatment, week 4, week 8, and week 16
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Method of measurement
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Based on Western Ontario and McMaster Universities Arthritis Index (WOMAC)
3
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Description
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Knee stiffness
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Timepoint
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Before treatment, week 4, week 8, and week 16
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Method of measurement
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Based on Western Ontario and McMaster Universities Arthritis Index (WOMAC)
4
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Description
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Blood level of immunologic factors VEGF IL23 IL17
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Timepoint
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Before studying and week 8
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Method of measurement
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Blood samples from patients will be taken for immunological tests before the study and at week 8. The blood samples will be stored at -80 degrees in the reference lab so they can be used for future studies as well.
Secondary outcomes
1
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Description
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Quality of life
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Timepoint
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Before treatment, week 4, week 8, and week 16
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Method of measurement
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Based on Short Form (36) Health Survey (SF 36)
2
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Description
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The need for using painkillers
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Timepoint
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Before treatment, week 4, week 8, and week 16
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Method of measurement
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Based on the patient's medical history as well as the form listing the painkillers used by the patient
3
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Description
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Side effects
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Timepoint
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Week 4, week 8, and week 16
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Method of measurement
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Based on the patient's medical history as well as the form about side effects filled out by the patient
Intervention groups
1
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Description
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First Intervention group: Manual acupuncture twice a week for 8 weeks
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Category
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Treatment - Devices
2
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Description
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Second Intervention group: Laser acupuncture twice a week for 8 weeks
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Category
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Treatment - Devices
3
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Description
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Control group: Sham laser twice a week for 8 weeks
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Category
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Placebo
1
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Sponsor
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Grant name
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Grant code / Reference number
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Is the source of funding the same sponsor organization/entity?
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Yes
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Title of funding source
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Mashhad University of Medical Sciences
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Proportion provided by this source
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100
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Public or private sector
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Public
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Domestic or foreign origin
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Domestic
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Category of foreign source of funding
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empty
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Country of origin
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Type of organization providing the funding
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Academic
Sharing plan
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Deidentified Individual Participant Data Set (IPD)
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Undecided - It is not yet known if there will be a plan to make this available
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Study Protocol
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Undecided - It is not yet known if there will be a plan to make this available
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Statistical Analysis Plan
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Undecided - It is not yet known if there will be a plan to make this available
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Informed Consent Form
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Undecided - It is not yet known if there will be a plan to make this available
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Clinical Study Report
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Undecided - It is not yet known if there will be a plan to make this available
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Analytic Code
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Undecided - It is not yet known if there will be a plan to make this available
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Data Dictionary
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Undecided - It is not yet known if there will be a plan to make this available