A study on pre-operative Misoprostol in reducing blood loss in total abdominal hysterectomy
Phase 4
Completed
- Conditions
- Health Condition 1: null- operative blood loss in total abdomonal hysterectomy (TAH)
- Registration Number
- CTRI/2011/091/000216
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Symptomatically women undergoing TAH for various benign gynaecological deseases
Exclusion Criteria
Any contraindication to misoprostol including mitral stenosis, glaucoma, diastolic blood pressure above 100mm of Hg, asthma, known allergic to prostaglandins
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method