Protocol summary
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Study aim
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The aim of this study is to determine the effects of zinc supplementation on insulin resistance and lipid profiles in women with polycystic ovary syndrome (PCOS).
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Design
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Study design: Parallel double-blind (both patients and researchers) randomized controlled clinical trial. Random assignment will be done by the use of computer-generated random numbers.
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Settings and conduct
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Population and sample size: 52 women with PCOS eligible and referred to Naghavi Clinic affiliated to Kashan University of Medical Sciences, Kashan, Iran in the study will be selected.
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Participants/Inclusion and exclusion criteria
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Inclusion criteria: Patients with polycystic ovary syndrome and aged 18 to 40 years will be included in this study. Exclusion criteria: Menopause, consume zinc supplements in the last 3 months, smokers, pregnancy, history of diseases including diabetes, liver, kidney and CVD, thyroid disorders, hyperprolactinemia and Cushing’s syndrome.
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Intervention groups
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Intervention: Patients will be assigned to receive either 50 mg zinc supplement (intervention group: n=26) or placebo (control group: n=26).
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Main outcome variables
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Outcomes: Markers of insulin metabolism (primary outcomes) and lipid profiles (secondary outcome) will be quantified at study baseline and end-of-trial.
General information
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Reason for update
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Due to an error, the request for an update in our website was conducted after paper published. However, the revisions were accordance with either the original approved proposal or with coordination with Vice Chancellor of Research at the University.
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Acronym
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IRCT registration information
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IRCT registration number:
IRCT201406075623N19
Registration date:
2014-07-16, 1393/04/25
Registration timing:
retrospective
Last update:
2019-10-25, 1398/08/03
Update count:
1
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Registration date
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2014-07-16, 1393/04/25
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Registrant information
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Recruitment status
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Recruitment complete
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Funding source
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Kashan University of Medical Sciences
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Expected recruitment start date
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2014-07-07, 1393/04/16
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Expected recruitment end date
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2014-07-16, 1393/04/25
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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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Effects of zinc supplementation on insulin resistance and lipid factors in women with polycystic ovary syndrome
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Public title
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Effect of supplementation in treatment of polycystic ovary syndrome
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Purpose
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Treatment
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Inclusion/Exclusion criteria
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Inclusion criteria:
Patients with PCOS according to Rotterdam criteria
Women aged 18-40 years
Exclusion criteria:
Menopause
Consume zinc supplements in the last 3 months
Smokers
Pregnancy
History of diseases including diabetes, liver, kidney and CVD.
Thyroid disorders
Hyperprolactinemia
Cushing’s syndrome
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Age
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From 18 years old to 40 years old
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Gender
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Female
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Phase
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3
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Groups that have been masked
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- Participant
- Investigator
- Outcome assessor
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Sample size
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Target sample size:
52
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Randomization (investigator's opinion)
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Randomized
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Randomization description
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At study baseline and after stratification for pre-intervention BMI and age, subjects will be randomly divided into two groups to take zinc supplementation (n=26) or placebo (n=26). Randomization will be done by the use of computer-generated random numbers.
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Blinding (investigator's opinion)
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Double blinded
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Blinding description
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Participants, investigators or the assessors of the outcomes are unaware of the study groups.
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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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2014-07-06, 1393/04/15
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Ethics committee reference number
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1682/1/5/29/پ
Health conditions studied
1
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Description of health condition studied
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Polycystic ovary syndrome
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ICD-10 code
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E28.2
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ICD-10 code description
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Sclerocystic ovary syndrome Stein-Leventhal syndrome
Primary outcomes
1
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Description
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Insulin resistance
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Timepoint
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Baseline and End-of-trial
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Method of measurement
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Elisa
2
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Description
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Insulin
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Timepoint
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Baseline and End-of-trial
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Method of measurement
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Elisa
3
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Description
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Insulin sensitivity
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Timepoint
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Baseline and End-of-trial
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Method of measurement
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Elisa
Secondary outcomes
1
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Description
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Fasting blood sugar
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Timepoint
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Baseline and End-of-trial
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Method of measurement
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Enzymatic kit
2
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Description
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Triglycerides
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Timepoint
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Baseline and End-of-trial
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Method of measurement
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Enzymatic kit
3
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Description
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HDL-cholesterol
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Timepoint
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Baseline and End-of-trial
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Method of measurement
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Enzymatic kit
4
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Description
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Total cholesterol
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Timepoint
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Baseline and End-of-trial
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Method of measurement
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Enzymatic kit
5
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Description
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LDL
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Timepoint
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Baseline and End-of-trial
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Method of measurement
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Enzymatic kit
6
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Description
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VLDL
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Timepoint
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Baseline and End-of-trial
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Method of measurement
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Enzymatic kit
Intervention groups
1
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Description
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Intervention group: Zinc tablet, 50 mg, daily, for 8 weeks orally.
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Category
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Treatment - Drugs
2
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Description
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Control group: Placebo tablet, daily, for 8 weeks orally.
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Category
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Treatment - Drugs
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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Kashan 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