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COMPLETED Phase 4

The SLIM Study: Sling and Botox® Injection for Mixed Urinary Incontinence

NCT02678377 · View on ClinicalTrials.gov ↗

Study Summary

This double-blind randomized controlled trial seeks to find a better treatment for women with mixed urinary incontinence (both stress and urgency incontinence). The primary aim is to determine whether midurethral sling surgery combined with injections of onabotulinumtoxinA (Botox®) into the detrusor muscle of the bladder improves symptoms of mixed urinary incontinence better than sling surgery alone.

Interventions

  • DRUG OnabotulinumtoxinA (Botox ®) Injections
  • DRUG Saline Injections

Study Locations (1)

Illinois

  • Northwestern Medicine Integrated Pelvic Health Clinic — Chicago

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2016-02
Est. Completion 2021-07-26
Phase Phase 4

Sponsor

Northwestern University

1,033 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02678377

The ClinicalTrials.gov registry entry for NCT02678377 describes a study currently listed as completed. It is categorized as Phase 4, 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 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwestern University, which has 1,033 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 Stress Urinary Incontinence appearing as the primary indexed condition, and to 2 interventions — of which OnabotulinumtoxinA (Botox ®) Injections 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: NCT02678377 reports 1 study location spanning 1 distinct geographic area — top geographies include Illinois. 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 NCT02678377 about?

NCT02678377 is a clinical study titled "The SLIM Study: Sling and Botox® Injection for Mixed Urinary Incontinence". This double-blind randomized controlled trial seeks to find a better treatment for women with mixed urinary incontinence (both stress and urgency incontinence). The primary aim is to determine whether midurethral sling surgery combined with injections of onabotulinumtoxinA (Botox®) into the detrusor...

What is the current status of trial NCT02678377?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2016-02. Estimated completion is 2021-07-26.

What conditions does trial NCT02678377 study?

This clinical trial studies the following conditions: Stress Urinary Incontinence, Mixed Urinary Incontinence, Urgency Incontinence. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02678377?

The interventions under investigation include: OnabotulinumtoxinA (Botox ®) Injections (DRUG), Saline Injections (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02678377?

This trial is sponsored by Northwestern University, which has 1,033 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02678377 being conducted?

This trial has 1 study location across Illinois. 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