Paperless Partograph for Management of Low Risk Labor

Normal Labor Clinical Trial

Official title:

A Randomized Clinical Trial of Paperless Versus Modified World Health Organization Partograph in Management of First Stage of Labour

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02714270
• Other study ID #: WHOP-PP
• Status: Completed
• Phase: N/A
• Start date: December 2016
• Est. completion date: June 2018

Study information

• Verified date: August 2018
• Source: Assiut University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Paperless partograph is a technique used for monitoring the progress of labor before delivery, and arriving at the accurate time to intervene for ensuring a safe delivery.

The study will be carried out to find out the effectiveness of paperless partograph in management of labor and its effect on maternal and neonatal outcomes

Recruitment information / eligibility

• Status: Completed
• Enrollment: 370
• Est. completion date: June 2018
• Est. primary completion date: March 2018
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 40 Years

Eligibility

Inclusion criteria:

1. Age: 18 to 40 years

2. Gestational age 38-42 weeks

3. Singleton pregnancy

4. Vertex presentation

5. Women who will accept to participate in the study

Exclusion criteria:

1. Malpresentation

2. Induced labour

3. Multiple pregnancy

4. Medical diseases with pregnancy

Related Conditions & MeSH terms

• Normal Labor

Intervention

Procedure:
• modified partograph

• paperless partograph

Locations

Country	Name	City	State
Egypt	Ahmed Abbas	Assiut	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Duration of active phase of labor	calculated in hours between cervical dilatation more than 3 cm till fully dilated	12 hours