Comparison between effect of two drugs on blood loss in patients undergoing abdominal myomectomy operatio
Phase 4
- Conditions
- Health Condition 1: D259- Leiomyoma of uterus, unspecifiedHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2024/01/061949
- Lead Sponsor
- Institute of Post Graduate Medical Education and Research and SSKM Hospital Kolkata
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Body weight between 50 - 90 kgs
2. Symptomatic leiomyomas and scheduled to undergo abdominal myomectomy
3. With number of myoma = 5
4. Myoma FIGO staging 3 to 6
Exclusion Criteria
1. Unwilling patient
2. Patients undergone vaginal or laparoscopic myomectomy
3. Patients received preoperative embolisation or GnRh analogue
4. Previous myomectomy
5. Pregnant and postmenopausal women
6. Myoma FIGO staging 1,2,7 & 8
7. Cervical and broad ligament myoma
8. Allergy or contraindications to Carbetocin such as coronary artery disease, asthma, epilepsy, migraine, kidney and hepatic diseases
9. Preoperative haemoglobin concentration less than 10 gm per d
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method