Investigation of PEMF Therapy for Female Patients With IC/BPS

Recruiting now · Not applicable · Has a placebo group

Conditions studied: Interstitial Cystitis, Chronic Interstitial Cystitis, Bladder Pain Syndrome

In brief

The purpose of this study is to gather information about the safety and effectiveness of the non-pharmacological (non-drug), non-invasive treatment known as low-frequency pulsed electromagnetic field (PEMF) therapy. The study team will distribute the PEMF device to female adults with Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) to measure its ability to decrease bladder and pelvic pain as well as other urinary symptoms associated with IC/BPS. There are two sequential Aims in this study and subjects will be recruited to participate in only one Aim. In both Aims, data will be collected at baseline/enrollment, 4-weeks after using PEMF therapy, and 8, 12, and 16 weeks post-enrollment.

Key facts

Study ID
NCT05149573
Run by
Wake Forest University Health Sciences
People needed
75
Starts
2022-08-29
Expected to finish
2027-02-01
Last updated by the study team
2026-05-07

Who can join

Age: 18 and older, up to 80. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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