Longitudinal Study Evaluating Recovery After Scheduled Cesarean Delivery

Mayo Clinic

Status: Completed

Conditions: Cesarean Section

Treatments: Other: Surveys

Study type: Observational

Funder types: Other

Identifiers

NCT04462107

19-012077

Details and patient eligibility

About

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

Enrollment: 66 patients

Sex: Female

Ages: 18 to 40 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Women 18 years of age or older who receive neuraxial anesthesia for elective cesarean delivery

Exclusion criteria

• Less than 18 years of age
• Gestational age less than 32 weeks
• Women whose infants have died or are in the neonatal intensive care unit after delivery
• Inability to read or understand written English
• Failed neuraxial anesthesia requiring general anesthesia

Trial design

66 participants in 1 patient group

Surveys

Description:

All participants will complete questionnaires at several time points, ranging from baseline to 3 months post partum.

Treatment:

Other: Surveys