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Recruiting NCT05750212

NCT05750212 Musculoskeletal and Pelvic Floor Health in Female Chronic Overlapping Pelvic Pain Conditions

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Clinical Trial Summary
NCT ID NCT05750212
Status Recruiting
Phase
Sponsor Loyola University
Condition Chronic Pelvic Pain Syndrome
Study Type OBSERVATIONAL
Enrollment 208 participants
Start Date 2023-01-24
Primary Completion 2025-09-24

Eligibility & Interventions

Sex Female only
Min Age 21 Years
Max Age 80 Years
Study Type OBSERVATIONAL
Interventions
ToneTendernessContraction

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 208 participants in total. It began in 2023-01-24 with a primary completion date of 2025-09-24.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this study is to learn about nerve function and pelvic muscle function. To do this we will compare the pelvic nerve and muscle function of women with chronic pelvic pain to those who do not have chronic pelvic pain. Understanding the pain may lead to better treatments in the future.

Eligibility Criteria

Inclusion Criteria: * Female sex * Age 21 to 80 years * Symptoms of CPP as defined by the American College of Obstetrics \& Gynecology (ACOG) for more than 6 months * At least two of seven overlapping CPP diagnosis (i.e., IC/PBS, IBS, Endometriosis, Vulvodynia, PN, FM, PFMP) * An average CPP pain score of at least three on a 10 point pain scale Exclusion Criteria: * Current or history of GI or GU pelvic cancer * Current pelvic infection (e.g., a UTI or vaginal infection) * Current or imminent planned pregnancy or recent delivery in the last 6 months * Abdominal or pelvic surgery in the last 36 months.

Contact & Investigator

Central Contact

Mary J Tulke, RN

✉ mtulke@luc.edu

📞 7082162067

Principal Investigator

Colleen Fitzgerald, MD

PRINCIPAL INVESTIGATOR

Loyola Medical Center

Frequently Asked Questions

Who can join the NCT05750212 clinical trial?

This trial is open to female participants only, aged 21 Years or older, up to 80 Years, studying Chronic Pelvic Pain Syndrome. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05750212 currently recruiting?

Yes, NCT05750212 is actively recruiting participants. Contact the research team at mtulke@luc.edu for enrollment information.

Where is the NCT05750212 trial being conducted?

This trial is being conducted at Maywood, United States.

Who is sponsoring the NCT05750212 clinical trial?

NCT05750212 is sponsored by Loyola University. The principal investigator is Colleen Fitzgerald, MD at Loyola Medical Center. The trial plans to enroll 208 participants.

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