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Completed Phase 2 Interventional

Study of BOTOX Injections to Assess Change in Disease Activity and Adverse Events in Adult Female Participants With Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS)

ClinicalTrials.gov ID: NCT05141006

Public ClinicalTrials.gov record NCT05141006. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 19, 2026, 10:53 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Placebo-Controlled, Parallel Arm Study to Assess the Safety and Efficacy of a Single Treatment of BOTOX, Followed by an Optional Open-Label Treatment With BOTOX, in Female Subjects With Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS)

Study identification

NCT ID
NCT05141006
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
83 participants

Conditions and interventions

Interventions

  • BOTOX Drug
  • Placebo for BOTOX Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 28, 2022
Primary completion
Jul 4, 2024
Completion
Dec 5, 2024
Last update posted
May 5, 2025

2022 – 2024

United States locations

U.S. sites
40
U.S. states
15
U.S. cities
35
Facility City State ZIP Site status
Urology Centers of Alabama /ID# 243600 Homewood Alabama 35209
Urology Associates of Mobile, PA /ID# 255854 Mobile Alabama 36608-6705
Alliance for Multispecialty Research (AMR) - Mobile /ID# 241002 Mobile Alabama 36608
Sun Kim Urology /ID# 257566 Buena Park California 90621
Cedars-Sinai Medical Center /ID# 245786 Los Angeles California 90048
University of California, Los Angeles /ID# 245131 Los Angeles California 90095
Tri Valley Urology Medical Group /ID# 254918 Murrieta California 92562-4902
Inland Urology /ID# 255410 Pomona California 91767
UCSD Medical Center /ID# 244935 San Diego California 92103-8620
Prestige Medical Group /ID# 257564 Santa Ana California 92705
Hartford Healthcare Group - Farmington /ID# 241037 Farmington Connecticut 06032-1943
Medstar Health Research Institute /ID# 245371 Washington D.C. District of Columbia 20010
Manatee Medical Research Institute /ID# 243859 Bradenton Florida 34205-8626
Clinical Research Center FL /ID# 243961 Pompano Beach Florida 33060
Ochsner LSU Health Shreveport - Regional Urology. /ID# 241034 Shreveport Louisiana 71106
Bay State Clincial Trials, Inc /ID# 240848 Watertown Massachusetts 01890
Sheldon Freedman MD, ltd /ID# 241003 Las Vegas Nevada 89144
Western New York Urology Associates - Harlem Professional Park /ID# 241036 Cheektowaga New York 14225-2591
North Shore University Hospital /ID# 242594 New Hyde Park New York 11040
NYU Langone Medical Center /ID# 241090 New York New York 10016-6402
Columbia University Medical Center /ID# 241086 New York New York 10032-3729
Columbia University Medical Center /ID# 241087 New York New York 10032-3729
Crystal Run Healthcare - Warwick /ID# 241116 Warwick New York 10990-4105
Cleveland Clinic Avon Hospital /ID# 247221 Avon Ohio 44011-1172
The Christ Hospital /ID# 244800 Cincinnati Ohio 45219
Univ Hosp Cleveland /ID# 247228 Cleveland Ohio 44106
MetroHealth Medical Center /ID# 254812 Cleveland Ohio 44109
Wright State Physicians Obstetrics and Gynecology /ID# 241112 Oakwood Ohio 45409-1980
The Institute for Female Pelvic Medicine and Reconstructive Surgery - Allentown /ID# 241012 Allentown Pennsylvania 18103-3691
MidLantic Urology /ID# 240997 Bala-Cynwyd Pennsylvania 19004
Thomas Jefferson University Hospital /ID# 243703 Philadelphia Pennsylvania 19107
Medical University of South Carolina /ID# 242780 Charleston South Carolina 29425
Southern Shores Urogynecology /ID# 253316 Myrtle Beach South Carolina 29752
Chattanooga Research and Medicine /ID# 241092 Chattanooga Tennessee 37412-3964
Urology Associates PC - Nashville /ID# 242914 Nashville Tennessee 37209-4035
University of Texas Southwestern Medical Center /ID# 244931 Dallas Texas 75390-7208
Advances in Health, Inc. /ID# 240850 Pearland Texas 77854
Potomac Urology - Alexandria /ID# 243963 Alexandria Virginia 22311-1735
Specialists For Women - Hillpoint /ID# 242541 Suffolk Virginia 23434-7181
Urology of Virginia /ID# 240843 Virginia Beach Virginia 23462

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05141006, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 5, 2025 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05141006 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →