Effectiveness of Evening Primrose Oil for Induction of Labor
ConditionInduction of Labor
Trial statusNot yet recruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexFemale
Age18-35
SponsorAssiut University
About this trial
Effectivness of primrose oil in induction of labour .
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
pregenent of 38 weeks and longer
singleton pregenency
vertex presentation
indication of labor induction
Disqualifiers
women who delivered by classical cs or had a history of myomectomy , hysterscopic uterine surgery , or cervical surgery like conisation
women with multiple gestation
women with evidence of low implanted placenta by ultrasound
women with contraindication to misoprostol or vaginal delivery
Trial design
Design model
Parallel
Treatments tested in this trial
Evening Primrose Oil 1000 MG
DrugEvening primrose oil 1000mg vaginally plus misoprostal for induction of labor
Treatment groups
72 Participants
are divided into 2 treatment groupsGroup A: Evening primrose oil + misoprostolActive comparator 1 intervention
Group B: misoprostol onlyOther 1 intervention
Trial outcomes
Primary outcomes
1
The interval between induction of labor and delivery
comparing between the interval between induction of labor and delivery in two groups one is using evening primrose oil + misoprostol and the other using misoprostol only.
Time frame
induction of labor may take more than 24 hoursLocations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: