Caesarean SectionNCT07244354
Maternal Hypothermia After Caesarean Section - Implications for Postoperative Recovery
An observational study of Caesarean Section, run by Oslo University Hospital at 1 site in Norway.
Trial summary
The aim of the study is to assess patient reported outcomes after caesarean section using self report questionnaire. Read more about this study
- Who is it for?
- Ages 18 to 50 years, women only
- Conditions the study is for
- Caesarean Section
- What is being tested?
- Self report questionnaire
- How many people
- 700 participants
- Where
- 1 siteNorway
- Study dates
- 1 Jan 2026to 1 Nov 2030
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 50 years
- Women only
- Adult
Study population: Females giving birth through caesarean section
Who may be able to join
- Exclusion Criteria: Stillborn baby, baby admitted to neonatal intensive care,
- -
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
About this study
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
- Conditions
- Caesarean Section
- Being tested
- Self report questionnaire
- Keywords
- patient reported outcome measures, quality of care, patient satisfaction, perioperative hypothermia, post caesarean infection
- Medical subject headings
- Patient Satisfaction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Self report questionnaireOther
No intervention
What is being measured
The primary outcome is the main question the study is designed to answer.
Patient reported recovery after caesarean delivery and symptoms of post caesarean infection
Data collection using questionnaire
Measured: Data collection 24 hours after surgery and 7 days after surgery and 30 days after surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Nov 2025
- Study start1 Jan 2026
- Primary completion1 Nov 2030 (estimated)
- Study completion1 Nov 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Caesarean SectionStudies of the same condition, open and under way.
- More trials run by Oslo University HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Other
- Enrolment
- 700 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Oslo University Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Elizabeth Reine, Oslo University Hospital
- Investigators
- Elizabeth Reine, PhD, Principal investigator, Oslo University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07244354
- Sponsor's protocol ID
- 911621
- Status last verified
- Jan 2026
- First submitted
- 17 Nov 2025
- Last updated
- 24 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 24 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Maternal Hypothermia After Caesarean Section - Implications for Postoperative Recovery
- ClinicalTrials.gov ID
- NCT07244354
- Acronym / sponsor ID
- 911621
- Conditions
- Caesarean Section
- Keywords
- patient reported outcome measures, quality of care, patient satisfaction, perioperative hypothermia, post caesarean infection
- Study type
- Observational
- Recruitment status
- Enrolling by invitation
- Enrolment
- 700 participants (estimated)
- Lead sponsor
- Oslo University HospitalUniversity, hospital or other
- Study start
- 1 Jan 2026 (actual)
- Primary completion
- 1 Nov 2030 (estimated)
- Study completion
- 1 Nov 2030 (estimated)
- First posted
- 24 Nov 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of the study is to assess patient reported outcomes after caesarean section using self report questionnaire.
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
Study design
- Observational model
- Other
- Time perspective
- Other
Who may qualify
- Ages
- 18 to 50 years
- Sex
- Female only
- Age groups
- Adult
- Study population
- Females giving birth through caesarean section
Key inclusion criteria (2 listed)
- Exclusion Criteria: Stillborn baby, baby admitted to neonatal intensive care,
- -
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Self report questionnaireNo intervention | Other | – |
Primary outcome
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
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Jul 2026.
- Individual participant dataSharing planned: Undecided
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Ultrasound Assessment Of Gastric Volume In Pregnant Women Undergoing Elective Cesarean Section
Gestational Diabetes Mellitus (GDM), Obstetric Anesthesia
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Effect of Dexmedetomidine on Postoperative Pain in Spinal Anesthesia for Cesarean Section at Assuit University Hospital
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Active, not recruiting
Implementation of a Disparities in Labor Outcomes Dashboard
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Ketamine Pharmacokinetics and Pharmacodynamics for Postpartum Depression and Pain After Cesarean Delivery
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Elizabeth Reine, PhD principal investigator
Oslo University Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Caesarean Section, run by Oslo University Hospital at 1 site in Norway.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: enrolling by invitation, as of the sponsor's last update on 24 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Norway. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
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). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jul 2026.