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NCT03121274 Clinical Trial

Early Versus Delayed Pushing in the Second Stage of Labor

Vaginal Delivery Clinical Trial

Official title:
Early Versus Delayed Pushing in the Second Stage of Labor

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03121274
Other study ID # 166
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 10, 2017
Est. completion date September 25, 2018

Study information
Verified date November 2018
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Nulliparous women in spontaneous or induced labour with term singleton pregnancy are randomized into two groups first group (early pushing) in this group patients were allowed to push within one hour after full cervical dilatation whether the vertex was visible or not. Second group (delayed pushing) patients here were asked not to push for maximum of 3 hours or start pushing when the vertex was visible.

Description:

Nulliparous women in spontaneous or induced labour with term singleton pregnancy are randomized into two groups first group (early pushing) in this group patients were allowed to push within one hour after full cervical dilatation whether the vertex was visible or not. Second group (delayed pushing) patients here were asked not to push for maximum of 3 hours or start pushing when the vertex was visible.

Oxytocin was allowed in both group and fetus was monitored with CTG.

Recruitment information / eligibility
Status Completed
Enrollment 184
Est. completion date September 25, 2018
Est. primary completion date August 1, 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 39 Years
Eligibility Inclusion Criteria:

- Healthy women

- Gestational age 36 to 40 weeks

- singleton pregnancy

Exclusion Criteria:

- women indicated for cesarean section

- Medical complications of pregnancy as hypertensive disorders or Diabetes Mellitus

- Fetal distress

- Epidural anaesthesia

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• vaginal delivery
vaginal delivery is carried by an expert obstetrician and the need for forceps or ventose is recorded

Locations
Country Name City State
Egypt Kasr Alainy medical school Cairo

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary successful vaginal delivery success of vaginal delivery within 3 hours from full cervical dilatation
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