IRCT201508259014N77CompletedPhase 2
Effect of painless vaginal delivery versus normal vaginal delivery on maternal and neonatal outcomes in pregnant women: a clinical trial
Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences0 sites168 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Sponsor
- Enrollment
- 168
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 15 years to 40 years (—)
- Sex
- Female
Inclusion Criteria
- •(a) gestational age of 37 weeks or over; (b) being eligible for vaginal delivery.
- •Exclusion criteria: (a) having diabetes, cardiovascular diseases, or intracranial diseases; (b) having gestational diabetes, preeclampsia, or macrosomia; (c) coagulation disorders; (d) dermal infection on the location of epidural anesthesia; (e) non-treated bacteremia.
Exclusion Criteria
- Not provided
Investigators
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