Clinical Trials Directory

Trials / Completed

CompletedNCT04462107

Longitudinal Study Evaluating Recovery After Scheduled Cesarean Delivery

Longitudinal Study Evaluating Postpartum Recovery After Scheduled Cesarean Delivery With the Obstetric Quality of Recovery Tool

Status
Completed
Phase
Study type
Observational
Enrollment
66 (actual)
Sponsor
Mayo Clinic · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The purpose of this research is to describe how patients recover after scheduled C-section for the first 3 months.

Conditions

Interventions

TypeNameDescription
OTHERSurveysAll participants will complete surveys that range in time from baseline to 3 months post partum.

Timeline

Start date
2021-02-01
Primary completion
2021-11-01
Completion
2021-11-01
First posted
2020-07-08
Last updated
2026-01-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04462107. Inclusion in this directory is not an endorsement.