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The Effect of Regenerative Peripheral Nerve Interface (RPNI) Surgery on Neuropathic Pain and Functional Outcomes in Major Lower Extremity Amputations

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

This prospective, observational cohort study evaluates the long-term outcomes of Regenerative Peripheral Nerve Interface (RPNI) surgery in patients with major lower extremity amputations suffering from symptomatic neuromas. RPNI is a surgical technique where the transected nerve end is implanted into a free autologous muscle graft to serve as a physiological target for reinnervation. The study aims to objectively assess the reduction in mechanical hypersensitivity using Pressure Pain Threshold (PPT) measurements via a digital algometer. Additionally, it monitors subjective neuropathic pain levels, functional mobility, and prosthesis satisfaction over a 24-month follow-up period compared to pre-operative baselines.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Age: Adults aged 18 to 70 years.

• Amputation Status: Unilateral major lower extremity amputation (Transtibial, Transfemoral, or Knee Disarticulation).

• Radiological Baseline: Absence of Heterotopic Ossification (HO) in the residual limb, confirmed by pre-operative X-rays (Walter Reed Classification Grade 0).

• Diagnosis: Confirmed diagnosis of Symptomatic Neuroma validated by the Clinical Triad:

‣ Neuropathic Pain: DN4 Questionnaire score ≥ 4.

⁃ Pain Intensity: Numeric Rating Scale (NRS) score ≥ 4.

⁃ Physical Exam: Positive Tinel's sign or palpation tenderness at a specific trigger point.

⁃ Radiology: Diagnostic Ultrasound visualization of the neuroma bulb.

• Surgical Indication: Scheduled for RPNI surgery as part of the routine standard of care treatment protocol due to prosthesis intolerance or severe pain.

• Consent: Willing and able to provide informed consent and attend follow-up visits.

Locations
Other Locations
Turkey
University of Health Sciences, Gulhane Training and Research Hospital, Department of Orthopedics and Traumatology
RECRUITING
Ankara
Contact Information
Primary
Ahmet Burak Bilekli, MD, Associate Professor
draburakbilekli@yahoo.com
+905326007020
Backup
Muhammed Burak Polat, MD
draburakbilekli@yahoo.com
+90 545 340 73 23
Time Frame
Start Date: 2026-01-20
Estimated Completion Date: 2030-03
Participants
Target number of participants: 20
Treatments
RPNI Group
Adult patients (18-70 years) with unilateral major lower extremity amputations (transtibial or transfemoral) who are diagnosed with Symptomatic Neuroma confirmed by the clinical triad (DN4 score ≥4, positive Tinel sign, and diagnostic ultrasound). These patients are scheduled to undergo Regenerative Peripheral Nerve Interface (RPNI) surgery as part of the routine standard of care treatment protocol.
Sponsors
Leads: Saglik Bilimleri Universitesi

This content was sourced from clinicaltrials.gov