Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Transcutaneous Tibial Nerve Stimulation for Spinal Cord Injury Neurogenic Bladder

NCT04350359 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine if electric stimulation to the leg, called transcutaneous tibial nerve stimulation (TTNS), can improve bladder outcomes in acute spinal cord injury.

Conditions Studied

Interventions

  • DEVICE Variable-dose TTNS Protocol 5 x week
  • DEVICE Fixed-dose TTNS Protocol
  • DEVICE Variable-dose TTNS Protocol 2 x week

Study Locations (2)

District of Columbia

  • MedStar National Rehabilitation Hospital — Washington D.C.

Texas

  • TIRR Memorial Hermann Research Center — Houston

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2020-06-08
Est. Completion 2026-07-01
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04350359

The ClinicalTrials.gov registry entry for NCT04350359 describes a study currently listed as recruiting. It is categorized as NA, 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 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 811 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Spinal Cord Injuries appearing as the primary indexed condition, and to 3 interventions — of which Variable-dose TTNS Protocol 5 x week 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: NCT04350359 reports 2 study locations spanning 2 distinct geographic areas — top geographies include District of Columbia, Texas. 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 NCT04350359 about?

NCT04350359 is a clinical study titled "Transcutaneous Tibial Nerve Stimulation for Spinal Cord Injury Neurogenic Bladder". The purpose of this study is to determine if electric stimulation to the leg, called transcutaneous tibial nerve stimulation (TTNS), can improve bladder outcomes in acute spinal cord injury.

What is the current status of trial NCT04350359?

This trial is currently recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2020-06-08. Estimated completion is 2026-07-01.

What conditions does trial NCT04350359 study?

This clinical trial studies the following conditions: Spinal Cord Injuries. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04350359?

The interventions under investigation include: Variable-dose TTNS Protocol 5 x week (DEVICE), Fixed-dose TTNS Protocol (DEVICE), Variable-dose TTNS Protocol 2 x week (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04350359?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 811 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04350359 being conducted?

This trial has 2 study locations across District of Columbia, Texas. 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