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

NCT ID: NCT06420453

Last Updated: 2024-05-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

300000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-01-01

Study Completion Date

2020-08-31

Brief Summary

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"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.

Detailed Description

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Conditions

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Birth Outcome, Adverse Labor Long Labor Complication Maternal Injury Maternal Distress During Labor and Delivery Neonatal and Perinatal Conditions Labor Duration

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Exposed to prolonged labor duration

No interventions assigned to this group

Not exposed to prolonged labor duration

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

All births with labor duration

Exclusion Criteria

Elective Cesarean birth
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Swedish Research Council

OTHER_GOV

Sponsor Role collaborator

Karolinska Institutet

OTHER

Sponsor Role lead

Responsible Party

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Mia Ahlberg

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Karolinska Institutet

Stockholm, , Sweden

Site Status

Countries

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Sweden

Other Identifiers

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2023-02010

Identifier Type: -

Identifier Source: org_study_id

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