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Enrolling by invitationNCT07244354Updated Jul 24, 2026

Maternal Hypothermia After Caesarean Section - Implications for Postoperative Recovery

An observational study in Caesarean Section, sponsored by Oslo University Hospital. Enrolling by invitation at 1 site in Norway. Open to female participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-07-24.

Sponsored by Oslo University Hospital · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
700
Ages
18 Years to 50 Years
Sex
Female
01

Study summary

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

Read the detailed description

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

02

Conditions studied

  • Caesarean Section

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Keywords

  • patient reported outcome measures
  • quality of care
  • patient satisfaction
  • perioperative hypothermia
  • post caesarean infection
03

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
Female
Sampling method
Non-probability sample

Study population

Females giving birth through caesarean section

Eligibility criteria

Inclusion Criteria: Caesarean section surgery -

Exclusion Criteria: Stillborn baby, baby admitted to neonatal intensive care,

-

04

Study design

Observational model
Other
Time perspective
Other
Enrollment
700 participants (estimated)
Patient registry
No

Interventions

  • OtherSelf report questionnaire

    No intervention

05

What researchers measure

Primary outcomes

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

    Data collection using questionnaire

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

06

Study locations

1 site
  • Oslo university hospital
    Oslo, Oslo, Norway
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07244354
Lead sponsor
Oslo University Hospital
Responsible party
Elizabeth Reine (Professional development and research nurse, Oslo University Hospital) — Principal investigator
First posted
Nov 24, 2025
Start date
Jan 1, 2026
Primary completion
Nov 1, 2030 (estimated)
Completion
Nov 1, 2030 (estimated)
Last update
Jul 24, 2026

Study contacts

Elizabeth Reine, PhD
principal investigator · Oslo University Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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