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Clinical Trial NCT07102654 for Amputation Stump, Amputation Neuroma, Amputation, Traumatic/Surgery, Amputation, Surgical is not yet recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here.
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Comparison Between Digital Nerve Microanastomosis and Traction Neurectomy in Post-Digital Amputation Pain 50 Observational

Not yet recruiting
Clinical Trial NCT07102654 is an observational study for Amputation Stump, Amputation Neuroma, Amputation, Traumatic/Surgery, Amputation, Surgical and is currently not yet recruiting. Enrollment is planned to begin on December 1, 2025 and continue until the study accrues 50 participants. Led by Centre hospitalier de l'Université de Montréal (CHUM), this study is expected to complete by July 1, 2026. The latest data from ClinicalTrials.gov was last updated on September 15, 2025.
Brief Summary

The goal of this prospective observational study is to assess the post-operative pain in adults with digital amputation following two different surgical interventions: microanastomosis of digital nerves or traction neurectomy. The main questions it aims to answer are:

  • Which surgical intervention results in less post-operative pain?
  • Which surgical intervention leads to fewer symptoms after six months?
  • Which sur...
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Official Title

Comparison Between Digital Nerve Microanastomosis and Traction Neurectomy in Post-Digital Amputation Pain: A Prospective Study

Conditions
Amputation StumpAmputation NeuromaAmputation, Traumatic/SurgeryAmputation, Surgical
Other Study IDs
  • 2026-13097
NCT ID Number
NCT07102654
Start Date (Actual)
2025-12-01
Last Update Posted
2025-09-15
Completion Date (Estimated)
2026-07-01
Enrollment (Estimated)
50
Study Type
Observational
Status
Not yet recruiting
Keywords
microanastomosis
traction neurectomy
digital amputation
digital nerve
Primary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
Postoperative Pain Measured by Visual Analog Scale in Adult Patients Following Digital Amputation
The primary objective of this study is to compare the level of postoperative pain associated with two surgical techniques: microanastomosis of digital nerves and traction neurectomy. Pain will be measured using the visual analog scale at one week, four weeks, and six months following the procedure. The visual analog scale ranges from 0 ( no pain) to 10 (worst imaginable pain).
1 week, 4 weeks and 6 months
Postoperative Symptoms Measured by the Disabilities of the Arm, Shoulder and Hand Questionnaire in Adult Patients Following Digital Amputation
The secondary objective of this study is to compare the level of postoperative symptoms associated with two surgical techniques: microanastomosis of digital nerves and traction neurectomy. The Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire will assess disability and hand-related symptoms at 6 months. The score ranges from 0 (no disability) to 100 (most severe disability)
6 months
Secondary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
Complication Rate of Microanastomosis of Digital Nerves and Traction Neurectomy in Adult Patients Following Digital Amputation
The tertiary objective of this study is to determine the incidence of postoperative complications for both microanastomosis of digital nerves and traction neurectomy.
1 week, 4 weeks, 6 months
Participation Assistant
Eligibility Criteria

Eligible Ages
Adult, Older Adult
Minimum Age
18 Years
Eligible Sexes
All
  • Age ≥ 18 years
  • Patients who have undergone a traumatic digital amputation
  • Patients treated with one of the two following techniques: microanastomosis of digital nerves or traction neurectomy
  • Postoperative follow-up of at least 6 months

  • Patients treated with a surgical intervention other than microanastomosis of digital nerves or traction neurectomy for digital amputation
  • Non-traumatic amputations (e.g., cancer or infection)
  • Follow-up of less than 6 months
  • Patients with pre-existing peripheral neuropathy
Centre hospitalier de l'Université de Montréal (CHUM) logoCentre hospitalier de l'Université de Montréal (CHUM)
No contact data.