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Study identifier: NCT07390591 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Patient and Caregiver Perspectives on Intravesical Instillations for Urinary Symptoms

Condition: Spinal Cord Injuries · Neurogenic Lower Urinary Tract Dysfunction · Neurogenic Bladder  ·  Sponsor: Medstar Health Research Institute

PhaseN/A
Planned participants60
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this observational qualitative study is to learn about the experiences and perspectives of patients with neurogenic lower urinary tract dysfunction (NLUTD) and their caregivers regarding different types of intravesical instillations used for urinary health. The study aims to understand the perceived benefits, challenges, and opportunities related to Lactobacillus-only, gentamicin-only, and combined gentamicin-Lactobacillus instillations. The main question this study seeks to answer is: 1\. Determine patient and caregivers' preferences, and overall experiences regarding intravesical therapeutics for urinary symptoms and UTI Researchers will compare responses from four groups: participants who have used Lactobacillus-only instillations, gentamicin-only instillations, combined gentamicin-Lactobacillus instillations, and caregivers who have experience supporting instillations. Participants will take part in a one-hour semi-structured interview and may be contacted for brief follow-up discussions to clarify findings. Interviews will be audio-recorded, transcribed, and analyzed using qualitative data software to identify themes related to treatment preferences and acceptability.

This description comes directly from the study's public registry record.

Talk to the study team

Christopher Riegner, MPH  ·  202-892-5857  ·  Christopher.R.Riegner@medstar.net

Inger Ljungberg, MPH  ·  202-877-1694  ·  Inger.H.Ljungberg@medstar.net

Always discuss trial participation with your own doctor first.

Locations (1)

Medstar National Rehabilitation HospitalWashington D.C., District of Columbia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07390591