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ACTIVE NOT RECRUITING Phase 1

Reduced-dose Botox for Urgency Incontinence Among Elder Females

NCT05512039 · View on ClinicalTrials.gov ↗

Study Summary

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.

Interventions

  • DRUG Botox 50 Unit Injection
  • DRUG Botox 100 Unit Injection

Study Locations (7)

Alabama

  • University of Alabama - Birmingham — Birmingham

California

  • Kaiser Permanente Medical Group — San Diego

Nebraska

  • University of Nebraska Medical Center — Omaha

New Hampshire

  • Dartmouth-Hitchcock Medical Center — Lebanon

Oregon

  • Oregon Health & Science University — Portland

Pennsylvania

  • University of Pittsburgh Medical Center — Pittsburgh

Texas

  • University of Texas Southwestern Medical Center — Dallas

Trial Details

FieldValue
Enrollment Target 376 participants
Start Date 2023-05-12
Est. Completion 2027-01-01
Phase Phase 1

Sponsor

Dartmouth-Hitchcock Medical Center

396 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05512039

The ClinicalTrials.gov registry entry for NCT05512039 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 376 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dartmouth-Hitchcock Medical Center, which has 396 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Overactive Bladder appearing as the primary indexed condition, and to 2 interventions — of which Botox 50 Unit Injection is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05512039 reports 7 study locations spanning 7 distinct geographic areas — top geographies include Alabama, California, Nebraska. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05512039 about?

NCT05512039 is a clinical study titled "Reduced-dose Botox for Urgency Incontinence Among Elder Females". 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.

What is the current status of trial NCT05512039?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 376 participants. The study started on 2023-05-12. Estimated completion is 2027-01-01.

What conditions does trial NCT05512039 study?

This clinical trial studies the following conditions: Overactive Bladder, Urgency Urinary Incontinence, Urinary Incontinence in Old Age. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05512039?

The interventions under investigation include: Botox 50 Unit Injection (DRUG), Botox 100 Unit Injection (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05512039?

This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 396 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05512039 being conducted?

This trial has 7 study locations across Alabama, California, Nebraska, New Hampshire, Oregon. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial