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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06420453
Enrollment
300000
Registered
2024-05-20
Start date
2008-01-01
Completion date
2020-08-31
Last updated
2024-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Brief 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.

Interventions

None listed

Sponsors

The Swedish Research Council
CollaboratorOTHER_GOV
Karolinska Institutet
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

All births with labor duration

Exclusion criteria

Elective Cesarean birth

Design outcomes

Primary

MeasureTime frame
Adverse neonatal outcomes1 month postpartum
Adverse maternal outcomes1 month postpartum

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026