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NCT05512039: RELIEF

Reduced-dose Botox for Urgency Incontinence Among Elder Females

Active, enrolled Phase 1, PHASE2 Last updated 3 February 2026
What this trial tests

Phase 1, PHASE2 trial testing Botox 50 Unit Injection in Overactive Bladder in 376 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
12 May 2023
Primary endpoint
1 September 2026
1 January 2027

Quick facts

Lead sponsorDartmouth-Hitchcock Medical Center
PhasePhase 1, PHASE2
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment376
Start date12 May 2023
Primary completion1 September 2026
Estimated completion1 January 2027
Sites7 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Dartmouth-Hitchcock Medical Center

Who can join

70 and older, female only, with Overactive Bladder or Urinary Incontinence in Old Age. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to study the treatment of urgency urinary incontinence (UUI), specifically among women 70 years and older, by comparing reduced versus standard dose of onabotulinumtoxinA (BTX; trade name BOTOX(c)) injection in the bladder.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Overactive Bladder

Currently open trials in the same condition.

Other Dartmouth-Hitchcock Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05512039.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing