EASE: The Materna Prep Pivotal Study
Enrolling By Invitation
99 years or below
Female
30 participants needed
1 Location
Brief description of study
This study is designed to evaluate the safety and effectiveness of the Materna Prep Device in reducing pelvic muscle injuries during vaginal delivery.
Eligible participants will be women ages 18+ scheduled for vaginal birth.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Medical Research,
-
Age: 99 years or below
-
Gender: Female
Updated on
04 Aug 2024.
Study ID: 849930
If you need assistance finding a non-cancer clinical research study or if you have any questions, please email psom-ocr@pobox.upenn.edu
For Cancer trials contact Penn Medicine's Cancer Trial Navigator at: PMCancerResearch@pennmedicine.upenn.edu or 215-349-8245