A Study to Evaluate Postpartum Recovery After Cesarean Delivery Using the Obstetric Quality of Recovery Tool

Overview

About this study

The purpose of this study is to describe the course of recovery over the first 3 months after elective cesarean delivery.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Women 18 years of age or older.
  • Patients who receive neuraxial anesthesia for elective cesarean delivery.
  • Singleton or multiple gestations.

Exclusion Criteria:

  • Age < 18 years old.
  • Gestational age < 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.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Emily Sharpe, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Additional contact information

Non-cancer trials contact form

Phone: 800-664-4542 (toll-free)

International patient clinical studies questions