A clinical trial comparing , Bupivacaine (local anesthetic )injection on either side of neck of uterus and vaginal stump left behind after total laparoscopic uterus removal versus vaginal stump injection of bupivacaine alone in reducing postoperative pain after total laparoscopic uterus removal.
Not Applicable
- Conditions
- Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecifiedHealth Condition 2: N859- Noninflammatory disorder of uterus, unspecifiedHealth Condition 3: N925- Other specified irregular menstruation
- Registration Number
- CTRI/2020/10/028207
- Lead Sponsor
- All India Institute Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Benign Gynecological conditions.
2.With or without salpingo oophorectomy.
3.Consenting women
Exclusion Criteria
1.Extensive additional tissue manipulation during surgery
2.Undue prolonged surgeries
3.Gynecological malignancies
4.Conversion to laparotomy
5.History of PID
6.Known allergy to amide anesthetics
7.Women not consenting to participate in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual Analog Scale of painTimepoint: 1 hour
- Secondary Outcome Measures
Name Time Method visual analog scale of painTimepoint: 2 hours and 6 hours