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NCT06420453 Clinical Trial

How Long Can Labor Last? Person Centred Care During Labor to Increase Safety for Women and Newborn

Labor Complication Clinical Trial

Official title:
How Long Can Labor Last? Person Centred Care During Labor to Increase Safety for Women and Newborn

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06420453
Other study ID # 2023-02010
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2008
Est. completion date August 31, 2020

Study information
Verified date May 2024
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

"How long will my labor last" is a very common question for midwives who care for women during birth. To evaluate safe labor duration largely determines management and care during birth. Today a standardized tool is used by midwives to evaluate normal and safe labor called the partograph. The World Health Organization partograph is a decision-making support tool designed to assist midwives in identifying normal labor duration and women at risk of developing complications. The tool guide the use of care interventions intended to mitigate any perceived risks. The partograph has been in use since the 1950ies and has had a profound impact on care and management during labor. Normal labor progression according to the partograph is a linear progression with cervical dilation of 1 centimeter per hour (alert line) and any deviation from this should lead to an intervention.The purpose of this research project is to increase person-centred care during labor. Specifically, we want to provide updated comprehensive information on labor duration and patient safety for reduction of; unnecessary medical interventions during normal labor; morbidity and mortality in the new-born; maternal complications during delivery and the puerperal period.

Recruitment information / eligibility
Status Completed
Enrollment 300000
Est. completion date August 31, 2020
Est. primary completion date August 31, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: All births with labor duration Exclusion Criteria: Elective Cesarean birth

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Sweden Karolinska Institutet Stockholm

Sponsors (2)
Lead Sponsor Collaborator
Karolinska Institutet The Swedish Research Council

Country where clinical trial is conducted

Sweden, 

Outcome
Type Measure Description Time frame Safety issue
Primary Adverse neonatal outcomes 1 month postpartum
Primary Adverse maternal outcomes 1 month postpartum
See also
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Recruiting NCT06261710 - Intrapartum Ultrasound in Labor: Sonography Only, Few Internal Examinations N/A
Completed NCT03276117 - Wide Use of Paperless Partograph in Evaluation of Labour N/A