NCT07244354

Brief Summary

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

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
700

participants targeted

Target at P75+ for all trials

Timeline
55mo left

Started Dec 2025

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress9%
Dec 2025Nov 2030

First Submitted

Initial submission to the registry

November 17, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

November 24, 2025

Completed
7 days until next milestone

Study Start

First participant enrolled

December 1, 2025

Completed
4.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2030

Last Updated

November 24, 2025

Status Verified

November 1, 2025

Enrollment Period

4.9 years

First QC Date

November 17, 2025

Last Update Submit

November 17, 2025

Conditions

Caesarean Section

Keywords

patient reported outcome measuresquality of carepatient satisfactionperioperative hypothermiapost caesarean infection

Outcome Measures

Primary Outcomes (1)

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

    Data collection using questionnaire

    Data collection 24 hours after surgery and 7 days after surgery and 30 days after surgery

Interventions

Self report questionnaireOTHER

No intervention

Eligibility Criteria

Age18 Years - 50 Years
Sexfemale
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Females giving birth through caesarean section

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Oslo university hospital

Oslo, Norway

Location

MeSH Terms

Conditions

Patient Satisfaction

Condition Hierarchy (Ancestors)

Treatment Adherence and ComplianceHealth BehaviorBehavior

Study Officials

  • Elizabeth Reine, PhD

    Oslo University Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Elizabeth Reine, PhD

CONTACT

004722119690uxelkl@ous-hf.no

Irene Brodshaug, MSc

CONTACT

004722119690

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professional development and research nurse

Study Record Dates

First Submitted

November 17, 2025

First Posted

November 24, 2025

Study Start

December 1, 2025

Primary Completion (Estimated)

November 1, 2030

Study Completion (Estimated)

November 1, 2030

Last Updated

November 24, 2025

Record last verified: 2025-11

Locations

NO(1)