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NCT06023498 · ClinicalTrials.gov registry record · NA
Optimizing Impact of Manual Therapy on Lumbar Spinal Stenosis
A NA study of Lumbar Spinal Stenosis, sponsored by University of Pittsburgh.
- Active
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 2
- Study locations
NCT06023498 is a NA study of Lumbar Spinal Stenosis that is active but no longer recruiting, run by University of Pittsburgh. The registered enrollment target is 60 participants, below the 666-participant average among 18 other Lumbar Spinal Stenosis trials with a reported enrollment target (91% lower). The trial reports 2 study locations across 2 states.
The verdict
NCT06023498, a NA study of Lumbar Spinal Stenosis, is active but no longer recruiting, sponsored by University of Pittsburgh.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 2
- Study locations
Study Summary
Lumbar spinal stenosis, a common condition in older adults, can cause pain and difficulty walking (i.e., intermittent neurogenic claudication - INC). Patients with INC not infrequently undergo spinal surgery that fails to help them 1/3-1/2 the time. The purpose of this multi-site feasibility study is to prepare for the conduct of a randomized controlled trial to test the efficacy of manual therapy, exercise, and intramuscular electroacupuncture in reducing pain and improving walking ability for those with INC, and ultimately limiting the need for surgical referrals.
Conditions Studied
Interventions
- OTHER Manual Therapy and Exercise
- OTHER Intramuscular Electroacupuncture
Study Locations (2)
Florida
- Orlando VA Medical Center - Orlando
Massachusetts
- Boston Medical Center - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2024-06-11 |
| Est. Completion | 2026-07-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06023498
The ClinicalTrials.gov registry entry for NCT06023498 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 666-participant average among 18 other Lumbar Spinal Stenosis trials with a reported enrollment target (91% lower). The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Lumbar Spinal Stenosis appearing as the primary indexed condition, and to 2 interventions - of which Manual Therapy and Exercise is the first listed.
NCT06023498 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Florida, Massachusetts.
Frequently Asked Questions
What is clinical trial NCT06023498 about?
NCT06023498 is a clinical study titled "Optimizing Impact of Manual Therapy on Lumbar Spinal Stenosis". Lumbar spinal stenosis, a common condition in older adults, can cause pain and difficulty walking (i.e., intermittent neurogenic claudication - INC). Patients with INC not infrequently undergo spinal surgery that fails to help them 1/3-1/2 the time. The purpose of this multi-site feasibility study i...
What is the current status of trial NCT06023498?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2024-06-11. Estimated completion is 2026-07-31.
What conditions does trial NCT06023498 study?
This clinical trial studies the following conditions: Lumbar Spinal Stenosis.
What interventions are being tested in trial NCT06023498?
The interventions under investigation include: Manual Therapy and Exercise (OTHER), Intramuscular Electroacupuncture (OTHER).
Who is sponsoring clinical trial NCT06023498?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06023498 being conducted?
This trial has 2 study locations across Florida, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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