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.

Scientific Rationale and Background Traditional "passive" nerve management techniques (e.g., traction neurectomy, burying in muscle/bone) often fail to prevent neuroma recurrence due to the lack of a physiological target for regenerating axons. This study investigates the long-term efficacy of the "Regenerative Peripheral Nerve Interface (RPNI)" technique. RPNI is an "active" surgical approach where the transected nerve end is implanted into a free autologous muscle graft to promote physiological reinnervation, thereby preventing chaotic axonal sprouting and neuroma formation.

Diagnostic Protocol (The Clinical Triad) To ensure accurate participant selection and strictly exclude non-neuroma pathologies such as Complex Regional Pain Syndrome (CRPS), the study employs a standardized "Clinical Triad" protocol for all potential candidates:

1. Neuropathic Validation: Confirmation of neuropathic pain character via validated questionnaires.
2. Anatomical Localization: Identification of a specific trigger point with a positive Tinel's sign triggering radiating paresthesia.
3. Radiological Confirmation: Visualization of the neuroma bulb at the symptomatic site using high-resolution Diagnostic Ultrasound.

Surgical Methodology (Standard of Care) Participants undergo the standard RPNI procedure as per the clinic's routine protocol.

• Graft Harvesting: A free autologous muscle graft (approx. 30x15x5 mm) is harvested. To minimize donor site morbidity, graft selection is standardized based on the amputation level: Vastus Lateralis for transtibial amputees and Biceps Femoris for transfemoral amputees.
• Inlay Technique: The neuroma bulb is excised, and the fresh nerve end is implanted into the center of the muscle graft using the "Inlay Technique" to maximize neurotization interface and minimize axonal escape.

Investigational Modules

• Viscero-Somatic Convergence: The study uniquely investigates the potential "cross-talk" mechanism between pelvic autonomic nerves (parasympathetic S2-S4) and somatic nerves. Participants are monitored for "Viscero-Somatic Symptoms," defined as stump pain triggered specifically by micturition, defecation, or sexual activity.
• Phantom Motor Execution (PME): As a functional indicator of reinnervation, patients are assessed for the ability to voluntarily execute movements with their phantom limb.

Sample Size and Power Analysis Based on a priori power analysis using G*Power 3.1 software, the sample size was calculated referencing the pressure pain threshold (PPT) effect sizes reported in comparable literature (Kubiak et al., 2022). Assuming a large effect size (Cohen's d = 1.5), an alpha error of 0.05, and a power of 90% (1-beta), a minimum of 13 participants is required to detect statistical significance. To account for a potential 20% dropout rate over the 24-month follow-up, the target enrollment is set at 20 patients.

Statistical Analysis Plan Data analysis will be performed using IBM SPSS Statistics 26.0.

• Normality Testing: The Shapiro-Wilk test will be used to determine the distribution of continuous variables.
• Longitudinal Analysis: The Friedman Test will be employed to analyze changes in dependent variables (NRS, DN4, PPT, PEQ scores) across the five time points (Pre-op, 3, 6, 12, 24 months).
• Pairwise Comparisons: Significant differences identified by the Friedman test will be further analyzed using the Wilcoxon Signed-Rank Test with Bonferroni correction.
• Correlation: Spearman's correlation analysis will be used to assess the relationship between objective algometer measurements and subjective prosthesis usage time (DPUT).
• Significance Level: A p-value of <0.05 will be considered statistically significant.

Inclusion Criteria:

• 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:

  1. Neuropathic Pain: DN4 Questionnaire score ≥ 4.
  2. Pain Intensity: Numeric Rating Scale (NRS) score ≥ 4.
  3. Physical Exam: Positive Tinel's sign or palpation tenderness at a specific trigger point.
  4. 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.

Exclusion Criteria:

• CRPS: Diagnosis of Complex Regional Pain Syndrome (CRPS Type 1 or 2).
• Concurrent Bone Surgery: Patients requiring simultaneous stump revision surgery (e.g., bone shortening, osteotomy, spur excision) or having existing HO (Walter Reed Grade > 0).
• Systemic Conditions: Uncontrolled diabetes mellitus (HbA1c > 8.5%) or severe peripheral arterial disease compromising wound healing.
• Cognitive Status: Cognitive impairment or psychiatric conditions preventing reliable completion of patient-reported outcome measures (PEQ, DN4).
• History: Previous RPNI surgery at the same site (Recurrent RPNI cases).

Adult patients with major lower extremity amputations presenting to the tertiary Orthopedics and Traumatology clinic with complaints of chronic residual limb pain, phantom limb pain, and prosthesis intolerance, who are diagnosed with symptomatic neuroma and scheduled for surgical intervention.

A formal plan for sharing individual participant data (IPD) has not yet been established. The investigators intend to evaluate the feasibility of sharing anonymized data upon reasonable request to the Principal Investigator following the publication of study results. However, a final decision will depend on strict compliance with local data protection regulations (KVKK) and institutional ethical approval mechanisms regarding data transfer. Currently, no specific public repository has been designated.