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NCT06324344 · ClinicalTrials.gov registry record · NA

Transcutaneous Electrical Nerve Stimulation (TENS) for Chemotherapy Induced Peripheral Neuropathy (CIPN)

A NA study, sponsored by Baylor College of Medicine.

Terminated
Registry status
NA
Development phase
10
Enrollment target

NCT06324344 is a NA study that was terminated before completion, run by Baylor College of Medicine. The registered enrollment target is 10 participants.

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The verdict

NCT06324344, a NA study, was terminated before completion, sponsored by Baylor College of Medicine.

TERMINATED
Registry status
NA
Development phase
10 participants
Enrollment target

Study Summary

The purpose of this pilot study is to examine the acceptability and proof of concept effectiveness of a wireless Transcutaneous Electrical Nerve Stimulation (TENS) technology to address Chemotherapy Induced Peripheral Neuropathy (CIPN). Participants, who satisfy the inclusion and exclusion criteria and sign the informed consent form will be randomly assigned with ratio of 1:1 into two groups. The patients and clinicians will be blinded for group allocation. One group will utilize TENS high-dose devices (Intervention group, IG); the other group will utilize low-dose TENS devices (Placebo group, PG). The baseline measurements will be performed, and the patients will take the programmed device home for a duration of 8 weeks. Then, the patients will come back after four weeks (4W) and after 8 weeks (8W) for outcome assessment. The primary outcome will be pain. Secondary outcomes include: nerve conduction and velocity, vibration perception threshold, quality of life. Exploratory outcomes include gait assessment (gait speed, stride length, double stance, and gait steadiness), and balance.

Interventions

  • DEVICE High-Dose TENS
  • DEVICE Low-Dose TENS

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2023-10-02
Est. Completion 2024-09-01
Phase NA

Sponsor

Baylor College of Medicine

616 total trials

What the Registry Record Tells You About NCT06324344

The ClinicalTrials.gov registry entry for NCT06324344 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor College of Medicine, which has 616 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which High-Dose TENS is the first listed.

NCT06324344 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06324344 about?

NCT06324344 is a clinical study titled "Transcutaneous Electrical Nerve Stimulation (TENS) for Chemotherapy Induced Peripheral Neuropathy (CIPN)". The purpose of this pilot study is to examine the acceptability and proof of concept effectiveness of a wireless Transcutaneous Electrical Nerve Stimulation (TENS) technology to address Chemotherapy Induced Peripheral Neuropathy (CIPN). Participants, who satisfy the inclusion and exclusion criteria ...

What is the current status of trial NCT06324344?

This trial is currently terminated. It is a NA study. The enrollment target is 10 participants. The study started on 2023-10-02. Estimated completion is 2024-09-01.

What interventions are being tested in trial NCT06324344?

The interventions under investigation include: High-Dose TENS (DEVICE), Low-Dose TENS (DEVICE).

Who is sponsoring clinical trial NCT06324344?

This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.