Tramadol Versus Diclofenac for Reducing Pain Before Outpatient Hysteroscopy in Post Menopausal Women: A Randomized Double Blind Placebo Controlled Trial

NCT02425709 Phase 3 UNKNOWN

The purpose of this study is to compare the effectiveness of Tramadol and diclofenac in reducing pain during outpatient hysteroscopy in postmenopausal women. Postmenopausal women undergoing outpatient hysteroscopy in Cairo university will be divided into 3 groups, the first group will receive Tramadol 50 mg 1 hour before the procedure, the second group will receive diclofenac 50mg 1 hour before the procedure and the third will receive a placebo. Pain will be assessed by a visual analogue scale.

Details

Lead sponsor	Cairo University
Phase	Phase 3
Status	UNKNOWN
Enrolment	210
Start date	2015-04

Conditions

• Hysteroscopy
• Pain

Interventions

• Diclofenac
• Tramadol
• Placebo

Primary outcomes

• Pain during the procedure measured using a visual analogue scale — 5 minutes after starting the procedure
  Women will be asked to score their pain using a visual analogue scale
• Pain immediately after the procedure measured using a visual analogue scale — 1 minute after completing the procedure
  Women will be asked to score their pain using a visual analogue scale

Countries

Egypt