A trial to determine whether the use of stitches or the use of a electric device called bipolar vessel sealer to control bleeding during surgical removal of uterus through vaginal route offers better relief of pain after surgery.
Phase 4
- Conditions
- Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecified
- Registration Number
- CTRI/2019/07/020019
- Lead Sponsor
- Department of OBG
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
uterus upto 18 weeks size
Exclusion Criteria
uterus more than 18 weeks size
uterus with features of malignancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method post -operative pain will be scored on a visual analogue scale for pain. The values will be compared between two groupsTimepoint: post operative pain will be scored <br/ ><br>6th hourly for first 24 hours after surgery. <br/ ><br>Subsequently once every morning till discharge
- Secondary Outcome Measures
Name Time Method Both the groups will be compared for the incidence of any complications during and following vaginal hysterectomyTimepoint: From the time of incision for vaginal hysterectomy to the time of discharge of participant from hospital;Both the groups will be compared for the total amount of Blood lost during vaginal hysterectomy.Timepoint: from the start to end of vaginal hysterectomy;Both the groups will be compared for the total time required for performing vaginal hysterectomyTimepoint: from the time of incision to sign-out time for vaginal hysterectomy