← Back to Clinical Trials
Recruiting NCT06120231

NCT06120231 Pulse-Width Modulation

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06120231
Status Recruiting
Phase
Sponsor Dartmouth-Hitchcock Medical Center
Condition Spinal Fusion
Study Type INTERVENTIONAL
Enrollment 50 participants
Start Date 2023-12-01
Primary Completion 2026-06-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Pulse width modulation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 50 participants in total. It began in 2023-12-01 with a primary completion date of 2026-06-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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.

Eligibility Criteria

Inclusion Criteria: * A patient will be eligible for study participation once they have been booked for a surgery involving pedicle screw placement and intraoperative neuromonitoring. Exclusion Criteria: * The study excludes neonates, minors, pregnant women, prisoners and cognitively impaired patients.

Contact & Investigator

Central Contact

Beverly Allen, BS

✉ Beverly..A.Allen@hitchcock.org

📞 6036179909

Principal Investigator

Linton Evans, Dr.

PRINCIPAL INVESTIGATOR

Dartmouth-Hitchcock Medical Center

Frequently Asked Questions

Who can join the NCT06120231 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Spinal Fusion. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06120231 currently recruiting?

Yes, NCT06120231 is actively recruiting participants. Contact the research team at Beverly..A.Allen@hitchcock.org for enrollment information.

Where is the NCT06120231 trial being conducted?

This trial is being conducted at Lebanon, United States.

Who is sponsoring the NCT06120231 clinical trial?

NCT06120231 is sponsored by Dartmouth-Hitchcock Medical Center. The principal investigator is Linton Evans, Dr. at Dartmouth-Hitchcock Medical Center. The trial plans to enroll 50 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology