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Clinical Research Directory

Browse clinical research sites, groups, and studies.

2 clinical studies listed.

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Interstitial Cystitis/Painful Bladder Syndrome

Tundra lists 2 Interstitial Cystitis/Painful Bladder Syndrome clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT07839689

Aerobic Exercise and Connective Tissue Massage in Painful Bladder Syndrome

The goal of this clinical trial is to learn if aerobic exercise training and connective tissue massage, in addition to patient education, can help treat women with bladder pain syndrome. The main questions it aims to answer are: Does aerobic exercise training and connective tissue massage reduce bladder-related pain severity? Does this intervention improve urinary symptoms, pain sensitivity, central sensitization-related symptoms, psychological symptoms, and quality of life? Researchers will compare patient education plus aerobic exercise training and connective tissue massage with patient education alone to see if the combined physiotherapy program is more effective. Participants will: Receive patient education about bladder pain syndrome Be randomly assigned to one of two groups Receive either patient education alone or patient education together with aerobic exercise training and connective tissue massage for 8 weeks Complete assessments at the beginning of the study and after 8 weeks

Gender: FEMALE

Ages: 18 Years - Any

Updated: 2026-09-24

1 state

Bladder Pain Syndrome
Painful Bladder Syndrome
Painful Bladder Syndrome (PBS)
+2
WITHDRAWN

NCT07038512

Evaluation of Hyivy Floora in Managing Interstitial Cystitis/Bladder Pain Syndrome/High-tone Pelvic Floor Dysfunction

The purpose of this study is to test the safety and effectiveness of the Floora Pelvic Rehabilitation Vaginal Dilator in females with Interstitial Cystitis/ Bladder pain Syndrome (IC/BPS) and High-tome Pelvic Floor Dysfunction (HTPFD). After enrollment, participants will be given a Floora device and will be instructed to use the device at least three times per week for 12-weeks in the comfort of their home. Each session consists of 10 minutes of heat and 10 minutes of dilation. All participants will be required to attend 3 in-person clinic visits and there will be two follow-up phone-calls throughout the 16-week trial period.

Gender: FEMALE

Ages: 18 Years - 80 Years

Updated: 2026-08-28

Interstitial Cystitis/Painful Bladder Syndrome
Interstitial Cystitis, Chronic
High Tone Pelvic Floor Dysfunction