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Clinical Trials in the USA / NCT06867185
Recruiting Not applicable

Evaluating Therapeutic Electrical Stimulation to Improve Nerve Healing After Surgical Repair of Digital Nerve Injuries

NCT06867185 · tracked via the Priya Life Science USA tracker
Sponsor
Checkpoint Surgical Inc.
Phase
Not applicable
Started
2025-04-24
Last updated
2026-01-09

Condition(s) studied

Digital Nerve InjuryNerve InjuryNerve ReconstructionNerve TraumaDigital Nerve Lesion

Investigational drug(s) / intervention(s)

Brief Electrical Stimulation TherapyDigital Nerve Repair

Brief Electrical Stimulation Therapy: 10-minutes of electrical stimulation to repaired nerve

Digital Nerve Repair: Standard of care surgical repair of digital nerve injury as determined by health care provider.

Study summary

The goal of this clinical study is to evaluate if a period of electrical stimulation delivered during the surgical repair procedure can speed up nerve healing.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Age 18-80 years * Candidate for surgical intervention under general anesthesia. * Require primary nerve injury repair in at least 1 digital nerve. * Following resection, have a resulting nerve gap of ≤ 10mm. * Able to complete tension-free end-to-end direct repair, or repair with a conduit, autograft, or allograft with a length ≤15mm * Signed and dated informed consent form. Exclusion Criteria: * Severe comorbid conditions, such as arrhythmia or congestive heart failure, preventing surgery under general anesthesia. * Nerve repair occurring \>1 month post-injury. * Incomplete nerve transection. * Injury requiring replantation of target digit * Injury distal to the distal interphalangeal joint. * Injury proximal to branching into the proper or common digital nerves. * Injuries to both digital arteries of an affected digit. * History of neuropathy, diabetic neuropathy, or any other known neuropathy * History of chronic ischemic condition of the upper extremity * Cognitive impairment preventing the ability to provide consent, follow post-operative instructions, or complete clinical assessments.

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
Indiana Hand to Shoulder Center Indianapolis Indiana Recruiting
University of Missouri Department of Orthopaedic Surgery Columbia Missouri Recruiting
Washington University in St Louis, Department of Orthopedic Surgery St Louis Missouri Recruiting
The Ohio State Univeristy - Department of Plastic and Reconstructive Surgery Columbus Ohio Recruiting
Harborview Medical Center - University of Washington Seattle Washington Recruiting

More Checkpoint Surgical Inc. trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06867185 on ClinicalTrials.gov ↗ ← All trials in the USA