Effect of Lidocaine Gel for Pain Relief during Endometrial Sampling in Postmenopausal bleeding: Randomized Controlled Trial
Phase 2
Completed
- Conditions
- Post menopausal bleedingEndometrial samplingLidocaine jellyPain score
- Registration Number
- TCTR20231005003
- Lead Sponsor
- /A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 72
Inclusion Criteria
women who were diagnosed with post menopausal bleeding and were literate, mature, and stable enough to do the visual analog score (VAS).
Exclusion Criteria
1.allergy to lidocaine jelly
2.unstable vital signs for example systolic blood pressure (SBP) lower than 90 mmHg., diastolic blood pressure (SBP) lower than 60 mmHg., pulse rate more than 120 bpm.,
3.patient unconsciousness or unable to answer the question and pain score.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the pain score when finishing endometrial sampling finishing endometrial sampling VAS,the pain score when finishing the procedure for 10 min when finishing the procedure for 10 min VAS,the pain score when start endometrial sampling when start endometrial sampling VAS
- Secondary Outcome Measures
Name Time Method satisfied finishing the procedure for 10 min score (1-10)