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IRCT20100127003213N9 IRCT 2020-05-19 Shiraz University of Medical Sciences Survey of the effect of gabapentin on post-operative pain of shoulder rotator cuff surgery Survey of the effect of gabapentin on post-operative pain of shoulder rotator cuff surgery 2020-06-09 anticipated 60 Complete https://irct.ir/trial/46247 interventional Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Prevention, Randomization description: Balanced block randomization, Blinding description: The nurse prescribing the medication, the patient, and the data collector will be unaware of the patient's study group. 2-3 Shoulder rotator cuff surgery. Intervention 1: Intervention group: Patients in group G will receive 300 mg of gabapentin at 6 pm on the first day after surgery and 600 mg of gabapentin in divided doses at 6 am and 6 pm on the second and third days. Intervention 2: Control group: Patients in group P will receive one placebo on the first day after surgery at 6 pm and on the second and third days after taking placebo in two divided doses at 6 am and 6 pm. No - There is not a plan to make this available Justification or reason for not sharing IPD is Its against our policy.
public Samira Safari
Anesthesiology Department, Faghihi Hospital, Zand Street
Shiraz Iran (Islamic Republic of) 7156948623 +98 71 3647 4270 Safari.anest@gmail.com Shiraz University of Medical Sciences scientific Arash Farbood
Anesthesiology Department, Faghihi Hospital, Zand Street
Shiraz Iran (Islamic Republic of) 1564471948 +98 36474270 arashfarbood@yahoo.com Shiraz University of Medical Sciences Iran (Islamic Republic of) Patients undergoing shoulder rotator cuff surgery Age 30-65 years old (ASA) I-II 30 years 65 years Both Sensitivity to gabapentin History of hypertension Heart disease Liver and kidney disease Acute or chronic pain associated with other areas of the body Any dependence on narcotics and psychotropic drugs Continuous use of tranquilizers for depression and anxiety disorders and seizure disorders M75.1 Rotator cuff tear or rupture, not specified as traumatic Treatment - Drugs Placebo Intervention group: Patients in group G will receive 300 mg of gabapentin at 6 pm on the first day after surgery and 600 mg of gabapentin in divided doses at 6 am and 6 pm on the second and third days. Control group: Patients in group P will receive one placebo on the first day after surgery at 6 pm and on the second and third days after taking placebo in two divided doses at 6 am and 6 pm. Pain. Timepoint: The severity of pain is measured by Numeric Rating Scale , every 2 hours to 6 hours, and then every 6 hours to 24 hours. Method of measurement: Numeric Rating Scale (NRS). Shiraz University of Medical Sciences Approved 2020-01-21 Ethics committee of Shiraz University of Medical Sciences Vice chancellor of research,7th floor of central building of Shiraz University of Medical Sciences, Zand street Shiraz Fars Iran (Islamic Republic of)