A clinical trial to study the effects of two procedures, Total Laparoscopic Hysterectomy and Non-descent Vaginal Hysterectomy in patients with benign uterine pathologies
Not Applicable
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: N938- Other specified abnormal uterine and vaginal bleeding
- Registration Number
- CTRI/2024/06/069030
- Lead Sponsor
- Department of Obstetrics and Gynaecology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Diagnosis of benign uterine pathologies.
2. Uterine size not surpassing 16 weeks of gravid uterus size, with sufficient uterine mobility.
3. Those willing to provide informed consent.
Exclusion Criteria
1. Genital neoplasm, cancer, or malignancy
2. Any adnexal pathology
3. Acute pelvic inflammatory disease
4. Uterine prolapse– stage II and above
5. Those who had any medical issues that could have been made worse by pneumoperitoneum or the Trendelenburg position.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method