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NCT07417943 · ClinicalTrials.gov registry record · NA

Neuromodulation to Enhance Motor Function in HSP

A NA study of Hereditary Spastic Paraplegia, sponsored by Rahul Sachdeva.

Recruiting
Registry status
NA
Development phase
15
Enrollment target
1
Study location

NCT07417943 is a NA study of Hereditary Spastic Paraplegia that is actively recruiting participants, run by Rahul Sachdeva. The registered enrollment target is 15 participants, below the 253-participant average among 5 other Hereditary Spastic Paraplegia trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07417943, a NA study of Hereditary Spastic Paraplegia, is actively recruiting participants, sponsored by Rahul Sachdeva.

RECRUITING
Registry status
NA
Development phase
15 participants
Enrollment target
1
Study location

Study Summary

Hereditary spastic paraplegia (HSP) is a rare neurological condition that causes stiffness, weakness, and difficulty walking due to damage in the nerves that control movement. This study will test whether a noninvasive form of spinal cord stimulation, called transcutaneous spinal cord stimulation (tSCS), can improve walking and reduce muscle stiffness in adults with HSP. In this study, participants will receive tSCS twice a week for 8 weeks. The stimulation is delivered through self-adhesive electrodes placed on the skin over the lower back and does not require surgery. Each session will last about one hour. After the treatment period, participants will be followed for an additional 8 weeks without stimulation to see whether any improvements are maintained. Researchers will measure walking speed, walking endurance, muscle stiffness, and overall disease severity. Additional tests will explore changes in bladder and bowel function and muscle strength.

Interventions

  • DEVICE transcutaneous spinal cord stimulation

Study Locations (1)

Kentucky

  • University of Kentucky - Lexington

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2026-03-01
Est. Completion 2028-02-01
Phase NA

Sponsor

Rahul Sachdeva

1 total trials

What the Registry Record Tells You About NCT07417943

The ClinicalTrials.gov registry entry for NCT07417943 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 253-participant average among 5 other Hereditary Spastic Paraplegia trials with a reported enrollment target (94% lower). The listed sponsor is Rahul Sachdeva, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hereditary Spastic Paraplegia appearing as the primary indexed condition, and to 1 intervention - of which transcutaneous spinal cord stimulation is the first listed.

NCT07417943 reports 1 study location spanning 1 distinct geographic area - top geographies include Kentucky.

Frequently Asked Questions

What is clinical trial NCT07417943 about?

NCT07417943 is a clinical study titled "Neuromodulation to Enhance Motor Function in HSP". Hereditary spastic paraplegia (HSP) is a rare neurological condition that causes stiffness, weakness, and difficulty walking due to damage in the nerves that control movement. This study will test whether a noninvasive form of spinal cord stimulation, called transcutaneous spinal cord stimulation (t...

What is the current status of trial NCT07417943?

This trial is currently recruiting. It is a NA study. The enrollment target is 15 participants. The study started on 2026-03-01. Estimated completion is 2028-02-01.

What conditions does trial NCT07417943 study?

This clinical trial studies the following conditions: Hereditary Spastic Paraplegia.

What interventions are being tested in trial NCT07417943?

The interventions under investigation include: transcutaneous spinal cord stimulation (DEVICE).

Who is sponsoring clinical trial NCT07417943?

This trial is sponsored by Rahul Sachdeva, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07417943 being conducted?

This trial has 1 study location across Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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