Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Efficacy and Safety of Budesonide Foam for Participants With Active Mild to Moderate Ulcerative Proctitis or Proctosigmoiditis

ClinicalTrials.gov ID: NCT01008423

Public ClinicalTrials.gov record NCT01008423. 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 Oct 21, 2026, 9:49 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 Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Assess the Efficacy and Safety of Budesonide Foam (2 mg/25 mL BID for 2 Weeks, Followed by 2 mg/25 mL QD for 4 Weeks) Versus Placebo in Subjects With Active Mild to Moderate Ulcerative Proctitis or Proctosigmoiditis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to establish the efficacy profile of rectally administered budesonide foam, as compared to an equivalent volume of rectally administered placebo foam over the same dosing schedule, in participants who present with a diagnosis of active, mild to moderate, ulcerative proctitis (UP) or ulcerative proctosigmoiditis (UPS). During the study, eligible participants will be allowed to maintain previously established oral 5-aminosalicylic acid (5-ASA) treatment at doses up to 4.8 grams/day (g/day).

Study identification

NCT ID
NCT01008423
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
281 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Nov 20, 2009 (Actual)
Primary completion
Mar 18, 2013 (Actual)
Completion
Mar 18, 2013 (Actual)
Last update posted
Aug 14, 2019

2009 – 2013

United States locations

U.S. sites
62
U.S. states
27
U.S. cities
62
Facility City State ZIP Site status
Not listed Dothan Alabama — —
Not listed Mesa Arizona — —
Not listed Tucson Arizona — —
Not listed Little Rock Arkansas — —
Not listed Chula Vista California — —
Not listed Garden Grove California — —
Not listed Mission Hills California — —
Not listed Monterey California — —
Not listed Roseville California — —
Not listed San Francisco California — —
Not listed Lafayette Colorado — —
Not listed Bristol Connecticut — —
Not listed Hamden Connecticut — —
Not listed Altamonte Springs Florida — —
Not listed Cape Coral Florida — —
Not listed Hialeah Florida — —
Not listed North Miami Beach Florida — —
Not listed Winter Park Florida — —
Not listed Macon Georgia — —
Not listed Marietta Georgia — —
Not listed Suwanee Georgia — —
Not listed Moline Illinois — —
Not listed Davenport Iowa — —
Not listed Topeka Kansas — —
Not listed Metairie Louisiana — —
Not listed Annapolis Maryland — —
Not listed Hagerstown Maryland — —
Not listed Prince Frederick Maryland — —
Not listed Silver Springs Maryland — —
Not listed Chesterfield Michigan — —
Not listed Rochester Michigan — —
Not listed Tupelo Mississippi — —
Not listed St Louis Missouri — —
Not listed Egg Harbor New Jersey — —
Not listed Marlton New Jersey — —
Not listed Great Neck New York — —
Not listed Mineola New York — —
Not listed New York New York — —
Not listed North Massapequa New York — —
Not listed Stony Brook New York — —
Not listed Asheville North Carolina — —
Not listed Fayetteville North Carolina — —
Not listed Greensboro North Carolina — —
Not listed Jacksonville North Carolina — —
Not listed New Bern North Carolina — —
Not listed Raleigh North Carolina — —
Not listed Rocky Mount North Carolina — —
Not listed Wilmington North Carolina — —
Not listed Beachwood Ohio — —
Not listed Tulsa Oklahoma — —
Not listed Portland Oregon — —
Not listed Germantown Tennessee — —
Not listed Houston Texas — —
Not listed La Porte Texas — —
Not listed Pasadena Texas — —
Not listed Plano Texas — —
Not listed San Antonio Texas — —
Not listed Ogden Utah — —
Not listed West Valley City Utah — —
Not listed Chesapeake Virginia — —
Not listed Lynchburg Virginia — —
Not listed Monroe Wisconsin — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01008423, 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 Aug 14, 2019 · Synced Oct 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01008423 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →