Wide Use of Paperless Partograph in Evaluation of Labour (labourRecord)

September 6, 2017 updated by: ayman darder, Assiut University

Wide Using of Paperless Partograph in Evaluation of Labour

Paperless partograph wide using in labour room as simple tool in evaluation of labour

Study Overview

Status

Completed

Conditions

Detailed Description

Both world health organization ( WHO) PARTOGRAPH and modified world heath organization (WHO)PARTOGRAPH are too long labour tools in evaluation of labour so we need simple tool in evaluation of labour

Study Type

Observational

Enrollment (Actual)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Egypt
      • Assiut, Egypt, 71723
        • Faculity of Medicine ,in Assiut,Egypt
      • Assiut, Egypt, 71723
        • Faculity of Medicine Assiut University
      • Assiut, Egypt, 71723
        • Faculity of Medicine in Assiut,Egypt
      • Assiut, Egypt, 71723
        • Faculity of Medicine,in Assiut ,Egypt
      • Assiut, Egypt, 71723
        • Faculity of Medicine,in Assiut,Egypt
      • Assiut, Egypt, 71723
        • Faculity of Medicine

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

25 years to 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

the collected data wail be analyzed using the statistical package for social science (version 10.0 for windows,SPSS.

Description

Inclusion Criteria:

  • Spontaneous labour
  • cephalic presentation
  • pregnant 37 weeks up to full term

Exclusion Criteria:

  • mail_presentation
  • induced labour

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Progress of labour
Time Frame: up to 2 month
Cervical dilated 1 cm each hour
up to 2 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
New born
Time Frame: up to 1 month
Apgar scor at 1 minute and Apgar scor at 5 minutes
up to 1 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Assiut University

Investigators

  • Study Chair: mohamed khalaph, professor, assiut universty faculity of medicine
  • Principal Investigator: ahmad abass, professor, assiut university faclity of meficibe

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 2, 2017

Primary Completion (Actual)

August 21, 2017

Study Completion (Actual)

August 26, 2017

Study Registration Dates

First Submitted

September 4, 2017

First Submitted That Met QC Criteria

September 6, 2017

First Posted (Actual)

September 8, 2017

Study Record Updates

Last Update Posted (Actual)

September 8, 2017

Last Update Submitted That Met QC Criteria

September 6, 2017

Last Verified

September 1, 2017

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • paperless partograph

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Labor Pain

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Venezuela

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

3
Subscribe