Maternal Hypothermia After Caesarean Section - Implications for Postoperative Recovery

The aim of the study is to assess patient reported outcomes after caesarean section using self report questionnaire.

Enrolling by invitation

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Key information

Conditions

Caesarean Section Behavior Health Behavior Patient Satisfaction Treatment Adherence and Compliance

Age range

18 year–50 year

Sex eligibility

Female

Study type

Observational

Primary location

Oslo university hospital

Oslo, Norway

About this study

The project consists of two studies: Study 1 explores patient reported outcomes after caesarean section related to recovery and quality of care. Study 2 explores possible associations between perioperative hypothermia during caesarean section and postoperative infection

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Caesarean section surgery -

Exclusion criteria

Stillborn baby, baby admitted to neonatal intensive care,

Treatment and study plan

Self report questionnaire

Other

No intervention

Primary outcomes

Patient reported recovery after caesarean delivery and symptoms of post caesarean infection

Time frame: Data collection 24 hours after surgery and 7 days after surgery and 30 days after surgery

Data collection using questionnaire

Interested in participating?

Enrolling by invitation

Interested in participating?

Request Info

Sponsors and collaborators

Lead sponsor

Oslo University Hospital

Other

Registry information

Important dates

Study start: 2026
Primary completion: 2030
Study completion: 2030
First posted: Nov 24, 2025
Registry last updated: Jul 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed