CTRI/2024/03/064554
Not yet recruiting
Phase 3
Comparison of the efficacy of a combination of Intramuscular Oxytocin (10 IU) and Sublingual Misoprostol(600mcg) with Intramuscular Oxytocin alone for Active Management of the Third Stage of Labour following Singleton Emergency Caesarean delivery -A Randomised, Double-blinded, Placebo-Controlled Trial - NI
Jawaharlal Institute of Medical Education and Research0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: O720- Third-stage hemorrhage
- Sponsor
- Jawaharlal Institute of Medical Education and Research
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Pregnant women \= 18 years of age
- •2\. Gestational age \=37 weeks to 42 weeks
- •3\. Following singleton emergency lower segment caesarean
- •4\. Under regional anaesthesia
Exclusion Criteria
- •1\. Antepartum haemorrhage
- •2\. Pre\-existing bleeding disorders
- •3\. Coagulation disorders
- •4\. Fever (greater than 38degree C)
- •5\. Acute Gastroenteritis
- •6\. Known hypersensitivity to Oxytocin or Misoprostol
- •7\. Distressed due to labour pains to give informed consent
- •8\. Liver and Renal Impairment
- •9\. Severe Anaemia
- •10\. On Steroid therapy
Outcomes
Primary Outcomes
Not specified
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