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Clinical Trial

Pain Outcomes After Digital Amputation Using Tulavi Allay™ Nerve Cap

NCT: NCT06915662 · RECRUITING

NCT IDNCT06915662
StatusRECRUITING
Start Date2025-09-20
Completion2027-04

Brief Summary

In 2016, one in five individuals in the United States (US) experienced chronic pain, and approximately 40% of them suffered from neuropathic pain. The physical and emotional burden on patients results in costs of billions of dollars annually. Digital amputations affect over 23,000 people each year in the US and may lead to neuropathic pain and neuroma formation in the transected nerves. Previous studies have reported a 6.6% incidence of symptomatic neuroma, and more than 60% of these patients require surgery to reduce the negative impact on their daily living activities. To minimize neuroma formation after digital amputation, various techniques have been described, such as traction neurectomies (TN) and dorsal transpositions (DT), with and without nerve coaptation. However, it remains unclear whether these techniques improve patient-reported outcome measures in individuals undergoing this type of procedure. Previously published studies are descriptive in nature, focus on a single surgical technique, or include patients with established symptomatic neuromas. The only prospective trial on this topic was published in 2000 and compared two conventional techniques that have since been modified to better minimize neuroma formation or to reduce mechanical pressure by transposing the nerve ends to the dorsal aspect of the hand. However, that study used different scales to measure outcomes and did not incorporate aspects of pain that affect patients' emotional and social well-being. Currently, two randomized controlled trials are enrolling patients. One compares surgical techniques for the treatment of neuroma rather than its prevention. The other excludes digits with injuries located distal to the interphalangeal joints. Both studies focus on more complex surgical techniques. Given the extent of this problem, there has been recent innovation aimed at preventing neuroma formation. One promising product is the Tulavi Allay™ Nerve Cap, which has demonstrated encouraging results in basic science studies and anecdotally in early clinical use cases. In this study, the investigators have designed a prospective trial to assess the efficacy of the Tulavi Allay™ Nerve Cap when used to prevent symptomatic digital nerve neuroma following traumatic digital amputation.

Frequently Asked Questions

What is Pain Outcomes After Digital Amputation Using Tulavi Allay™ Nerve Cap?

Pain Outcomes After Digital Amputation Using Tulavi Allay™ Nerve Cap is a clinical trial registered under NCT06915662. Current status: RECRUITING.

What is the status of NCT06915662?

The current status of NCT06915662 (Pain Outcomes After Digital Amputation Using Tulavi Allay™ Nerve Cap) is: RECRUITING.

When did Pain Outcomes After Digital Amputation Using Tulavi Allay™ Nerve Cap start?

Pain Outcomes After Digital Amputation Using Tulavi Allay™ Nerve Cap started on 2025-09-20.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.