Peripheral Neuropathy Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults who were between 18 and 70 years old at the time of their nerve injury
- People who are willing to take part, attend all required follow-up appointments, and have signed a consent form after being fully informed about the study
- People who have completely lost feeling in a specific area of a finger due to a nerve injury
- People whose nerve injury is suitable for repair by joining the two ends of the nerve directly together with stitches
- People who have a cut nerve (or nerves) in a finger or thumb, located below the wrist, that affects feeling at the fingertip
- People whose treating surgeon considers them suitable for either standard nerve repair stitching or robotic-assisted nerve repair stitching
- People whose injury was treated within 10 days of it occurring
- People confirmed during surgery to have a nerve injury with no gap, where the nerve ends can be stitched directly together
Who may not be able to join:
- People who are unable or unwilling to give their informed consent to participate
- People with significant health conditions affecting the heart, digestive system, breathing, hormones, liver, or brain and nervous system, or with a history of mental health disorders, or other conditions that the investigator believes could affect the study results or the person's ability to follow the study requirements
- People who are currently taking part in another clinical research study that the investigator believes could affect their safety or results in this trial
- People considered part of a vulnerable group, such as pregnant women, or others the investigator determines should not participate for other reasons
- People who need nerve repair on both sides (both hands or both sides of the same hand) at the same time
- People who already had reduced or impaired feeling in the injured finger before the injury being studied
- People who have an implanted pacemaker
- People whose surgery involves reattaching a finger that also requires bone repair
- People where a condition is discovered during surgery that, in the surgeon's opinion, would make continued participation unsuitable (confirm with trial site for full details)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 8336646276
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Two-point discrimination (2PD) test, at 6-months post index procedure.; Intraoperative serious adverse event rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.