NCT04462107View on ClinicalTrials.gov

Longitudinal Study Evaluating Recovery After Scheduled Cesarean Delivery

CompletedOBSERVATIONAL

Enrollment

66

Participants

Timeline

Start Date

February 1, 2021

Primary Completion Date

November 1, 2021

Study Completion Date

November 1, 2021

Conditions

Cesarean Section

Interventions

OTHER

Surveys

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

Trial Locations (1)

55905

Mayo Clinic in Rochester, Rochester

Sponsors

Lead Sponsor

All Listed Sponsors

lead

Mayo Clinic

OTHER

NCT04462107 - Longitudinal Study Evaluating Recovery After Scheduled Cesarean Delivery | Biotech Hunter | Biotech Hunter