Trauma on Sexual Function and Dyspareunia Among Primiparous Patients

Overview

About this study

The purpose of this study is to investigate the maternal perception of birth trauma and its impact on sexual function and postpartum dyspareunia in a select cohort of patients status-post vaginal 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:

  • Adults aged >18, primiparous, operative or spontaneous vaginal delivery

Exclusion Criteria: 

  • Delivery via Cesarean

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 4/25/2024. Questions regarding updates should be directed to the study team contact.

 

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 Contact

Rochester, Minn.

Mayo Clinic principal investigator

Alyssa Larish, M.D.

Open for enrollment

Contact information:

Courtney McEwen M.D.

(507) 538-5809

McEwen.Courtney@mayo.edu

More information

Publications

Publications are currently not available