Labour Induction Clinical Trial
NCT number | NCT02168881 |
Other study ID # | Misoprostol-2014 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | June 19, 2014 |
Last updated | June 19, 2014 |
Start date | May 2014 |
This study is to compare between oral misoprostol in solution and vaginal dinoprostone in induction of labour in primiparous women with singleton pregnancy as regards efficiency and safety to both mother and fetus.
Status | Recruiting |
Enrollment | 342 |
Est. completion date | |
Est. primary completion date | January 2016 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Primigravida - >37 wks Exclusion Criteria: - Scarred uterus - Macrosomia |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label
Country | Name | City | State |
---|---|---|---|
Egypt | Ain Shams Maternity hospital | Cairo |
Lead Sponsor | Collaborator |
---|---|
Ain Shams University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | induction delivery time | 2 hourly | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
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