IRCT20100303003485N5CompletedPhase 3
The effect of sildenafil citrate on fetal distress during labor and cesarean section - a double-blind clinical trial with placebo
Rasht University of Medical Sciences0 sites104 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- Enrollment
- 104
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 40 years (—)
- Sex
- Female
Inclusion Criteria
- •Age between 18-40 years
- •Single pregnancy
- •Term pregnancy (37-41 weeks)
- •Normal fetal structure and without any anomalies
- •Cephalic presentation
- •Estimated weight above 2500 grams
- •Without CPD
- •Candidate for normal vaginal delivery
Exclusion Criteria
- •Drug reaction to Sildenafil
- •Fetal anomalies
- •Metabolic disorder
- •Cardiac disorders
- •Renal disorders
- •Visual disorders
- •Liver anomalies
- •Previous cesarean
- •Preeclampsia
- •Taking medications Nitrate
Investigators
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