CTRI/2023/10/059156
Not yet recruiting
Phase 2
Camparison of the efficacy of the combination of the Oxytocin and Rectal Misoprostol (600mcg) with Oxytocin alone for active manaegment of third stage labour following singleton vaginal delivery - A randomised, double binded, placebo-controlled trial (OxyPGE1 Trial) - OxyPGE1 Trial
Intramural Jawarharlal Institute of Postgraduate Medical Education and Research0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Intramural Jawarharlal Institute of Postgraduate 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 vaginal delivery
Exclusion Criteria
- •1\. Antepartum haemorrhage
- •2\. Pre\-existing bleeding disorders
- •3\. Fever ( \>38?C)
- •4\. Acute Gastroenteritis
- •5\. Known hypersensitivity to Oxytocin or Misoprostol
- •6\. Distressed due to labour pains to give informed consent
Outcomes
Primary Outcomes
Not specified
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