How Long Can Labor Last? Person Centred Care During Labor to Increase Safety for Women and Newborn - Trial NCT06420453
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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Study Focus
Sponsor & Location
Karolinska Institutet
Timeline & Enrollment
N/A
Jan 01, 2008
Aug 31, 2020
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
Data Source
ClinicalTrials.gov
NCT06420453
Non-Device Trial