Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06120231 · ClinicalTrials.gov registry record · NA
Pulse-Width Modulation
A NA study of Spinal Fusion and Spinal Stenosis, sponsored by Dartmouth-Hitchcock Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT06120231 is a NA study of Spinal Fusion and Spinal Stenosis that is actively recruiting participants, run by Dartmouth-Hitchcock Medical Center. The registered enrollment target is 50 participants, below the 481-participant average among 19 other Spinal Fusion trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06120231, a NA study of Spinal Fusion and Spinal Stenosis, is actively recruiting participants, sponsored by Dartmouth-Hitchcock Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
The overarching aim of this project is to modulate the pulse-width during stimulation of pedicle screws and record the response thresholds associated with each PWM setting. During this initial phase of the investigation, no further data will be collected.
Conditions Studied
Interventions
- DIAGNOSTIC_TEST Pulse width modulation
Study Locations (1)
New Hampshire
- Dartmouth-Health - Lebanon
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2023-12-01 |
| Est. Completion | 2027-06-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06120231
The ClinicalTrials.gov registry entry for NCT06120231 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 481-participant average among 19 other Spinal Fusion trials with a reported enrollment target (90% lower). The listed sponsor is Dartmouth-Hitchcock Medical Center, which has 427 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Spinal Fusion appearing as the primary indexed condition, and to 1 intervention - of which Pulse width modulation is the first listed.
NCT06120231 reports 1 study location spanning 1 distinct geographic area - top geographies include New Hampshire.
Frequently Asked Questions
What is clinical trial NCT06120231 about?
NCT06120231 is a clinical study titled "Pulse-Width Modulation". The overarching aim of this project is to modulate the pulse-width during stimulation of pedicle screws and record the response thresholds associated with each PWM setting. During this initial phase of the investigation, no further data will be collected.
What is the current status of trial NCT06120231?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2023-12-01. Estimated completion is 2027-06-01.
What conditions does trial NCT06120231 study?
This clinical trial studies the following conditions: Spinal Fusion, Spinal Stenosis.
What interventions are being tested in trial NCT06120231?
The interventions under investigation include: Pulse width modulation (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT06120231?
This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 427 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06120231 being conducted?
This trial has 1 study location across New Hampshire. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Spinal Fusion
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Photobiomodulation for Lower Back Pain Post Spinal Fusion and Decompression Surgery
RECRUITING · NA
-
Kids With Iron Deficiency and Scoliosis
RECRUITING · NA
-
Trans-Auricular Stimulation for Postoperative Inflammation in Spine Surgery
RECRUITING · NA
-
Postoperative Pain Control in AIS Using Liposomal Bupivacaine vs. 0.25% Bupivacaine With Epinephrine
RECRUITING · NA
-
Lumbar Fusion With Porous Versus Non-Porous Cages
ACTIVE NOT RECRUITING · NA
-
Alvimopan and Ileus in PSF
COMPLETED · NA
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
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.