Clinical Trials Logo

Cystitis clinical trials

View clinical trials related to Cystitis.

Filter by:
  • Enrolling by invitation  
  • Page 1

NCT ID: NCT06212661 Enrolling by invitation - Migraine Clinical Trials

Migraine Medication Effects on Urinary Symptoms

Start date: April 5, 2024
Phase:
Study type: Observational

A prospective observational cohort trial to study the effects of CGRP inhibitors (CGRPi) on lower urinary tract symptoms (LUTS) and bladder/pelvic pain. Candidates for either CGRPi or an alternative therapy for refractory migraines (OnabotulinumtoxinA (BoNTA) extracranial muscle injections) with baseline LUTS will be recruited. The investigators will assess LUTS and pelvic pain using validated symptom and quality-of-life questionnaires, pretreatment and at 3 months post-treatment follow-up, comparing change in symptoms based on treatment received.

NCT ID: NCT05551949 Enrolling by invitation - Clinical trials for Urinary Tract Infections

Preventing Recurrent UTI With Vaginal Estrogen

PRUVE
Start date: January 31, 2023
Phase: Phase 4
Study type: Interventional

Among postmenopausal women who suffer from recurrent urinary tract infections (UTI), vaginal estrogen therapy prevents UTI recurrences for 50% of sufferers. This research will investigate why some women benefit but others do not, focusing on (a) the effects of vaginal estrogen therapy on the bacteria that inhabit the vagina and bladder, (b) its influence on immune responses in both compartments, and (c) the extent to which those changes are critical to successful UTI prevention. The findings will be a first step in the development of more effective strategies to prevent UTI, one of the most common and costly benign urologic conditions.

NCT ID: NCT05456308 Enrolling by invitation - Clinical trials for Interstitial Cystitis

What is the Optimal Technique for Hydrodistention?

Start date: July 1, 2022
Phase: N/A
Study type: Interventional

This research study is being done to learn what is the best way to perform hydrodistention. Eligible participants will be enrolled and have follow-up for three months after surgery. The study team hypothesizes that changes in hydrodistention technique, including pressure, number of distention, and duration of distention, leads to no or minimal changes in symptom improvement for patients with Interstitial cystitis/bladder pain syndrome (IC/BPS).

NCT ID: NCT01301365 Enrolling by invitation - Clinical trials for Interstitial Cystitis

Autonomic Response During Cystodistension in Patients Suspected of Having Interstitial Cystitis

Start date: November 2010
Phase: N/A
Study type: Observational

The aim of this study is to check whether patients with cystoscopic findings supporting the diagnosis of Interstitial Cystitis (IC) have a higher autonomic response (change in blood pressure / pulse)than patients without cystoscopic findings.