NCT06420453

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

Name: Clinical Trial NCT06420453
Creator: Karolinska Institutet
Keywords: Birth Outcome, Adverse,Labor Long,Labor Complication,Maternal Injury,Maternal Distress During Labor and Delivery,Neonatal and Perinatal Conditions,Labor Duration, clinical trial, Sweden

Karolinska Institutet·ClinicalTrials.govCompleted

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Study focus

Disease/Condition: Birth Outcome, Adverse,Labor Long,Labor Complication,Maternal Injury,Maternal Distress During Labor and Delivery,Neonatal and Perinatal Conditions,Labor Duration
Study type: Observational

Sponsor & location

Primary sponsor: Karolinska Institutet
Location: Stockholm, Sweden

Timeline & enrollment

Phase: N/A
Start date: Jan 01, 2008
End date: Aug 31, 2020
Enrollment: 300000 participants

Primary outcome

Adverse neonatal outcomes,Adverse maternal outcomes

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.

ICD-10 classifications

Fetus and newborn affected by other specified complications of labour and deliveryFetus and newborn affected by maternal factors and by complications of pregnancy, labour and deliveryFetus and newborn affected by other complications of labour and deliveryOther specified complications of labour and deliveryMaternal distress during labour and delivery

Data source

Registry: ClinicalTrials.gov
Trial ID: NCT06420453
Type: Non-Device Trial

About this record

Access comprehensive clinical trial information for NCT06420453 through Pure Global AI's free database. This phase not specified trial is sponsored by Karolinska Institutet and is currently Completed. The study focuses on Birth Outcome, Adverse,Labor Long,Labor Complication,Maternal Injury,Maternal Distress During Labor and Delivery,Neonatal and Perinatal Conditions,Labor Duration. Target enrollment is 300000 participants.

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