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Median Nerve Decompression for Complex Regional Pain Syndrome: A Clinical Study

Surgical Treatment of Complex Regional Pain Syndrome by Median Nerve Decompression and Lesion-Specific Correction: A Clinical Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07263256
Acronym
CRPS-SURG
Enrollment
74
Registered
2025-12-04
Start date
2014-01-31
Completion date
2023-12-31
Last updated
2025-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Complex Regional Pain Syndrome I (CRPS I), Nerve Entrapment Syndrome

Keywords

Complex Regional Pain Syndrome, CRPS Type I, Neuropathic Pain, Median Nerve Decompression, Peripheral Nerve Surgery, Upper Limb Pain, Nerve Entrapment, Chronic Pain, Hand Surgery

Brief summary

This clinical study evaluates the effectiveness of surgical treatment in patients with upper-limb complex regional pain syndrome (CRPS) diagnosed according to the Budapest criteria. Seventy-four patients were assessed between 2014 and 2023. Patients with identifiable structural pathology underwent lesion-specific surgical correction, while those without detectable lesions but with neuropathic nocturnal pain underwent decompression of the median nerve. Pain intensity was measured using the visual analogue scale (VAS) preoperatively, at 10-12 days, and at three months. The study aims to determine the speed and magnitude of pain improvement after targeted surgical intervention.

Detailed description

Complex regional pain syndrome (CRPS) is a multifactorial neuropathic pain disorder that can occur after trauma or surgery and is often resistant to conservative treatment. Increasing evidence suggests that in a subset of patients, peripheral mechanical factors contribute significantly to symptom generation. This prospective clinical study evaluated the outcomes of targeted surgical treatment in patients with CRPS of the upper limb who met the Budapest diagnostic criteria. From 2014 to 2023, seventy-four patients were examined. Thirty-eight patients presented with identifiable structural pathology, such as hardware impingement, neuroma, tendon adhesion, or scar tethering, and underwent lesion-specific surgical correction. Thirty-six patients had no detectable structural lesion but reported nocturnal neuropathic pain suggestive of median nerve irritation; these patients underwent decompression of the median nerve. Pain intensity was measured using the visual analogue scale (VAS) before surgery, at suture removal (10-12 days), and at three months postoperatively. Patients with identifiable mechanical pathology demonstrated substantial improvement, with an average 7.2-point VAS reduction after six months. Patients who underwent median nerve decompression showed rapid and marked pain reduction, improving by 7.1 points within 10-12 days and 8.6 points within three months. Acute CRPS cases improved more than chronic ones, indicating an early therapeutic window before central sensitization becomes dominant. Only one chronic case failed to improve. The results suggest that timely surgical assessment and correction of peripheral nerve or soft-tissue factors may lead to rapid and significant clinical recovery in selected CRPS patients.

Interventions

PROCEDURELesion-Specific Surgical Correction

Surgical correction of identifiable structural pathology, including hardware impingement, neuroma, tendon adhesion, scar tethering, or other mechanical causes of complex regional pain syndrome of the upper limb.

PROCEDUREMedian Nerve Decompression

Surgical correction of identifiable structural pathology, including hardware impingement, neuroma, tendon adhesion, scar tethering, or other mechanical causes of complex regional pain syndrome of the upper limb.

Sponsors

Charles University, Czech Republic
CollaboratorOTHER
Ministry of Health, Czech Republic
CollaboratorOTHER_GOV
General University Hospital, Prague
CollaboratorOTHER
Jitka Fricova
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Parallel Assignment Group A: Lesion-specific correction Group B: Median nerve decompression

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed Complex Regional Pain Syndrome (CRPS) according to Budapest criteria * Age ≥ 18 years * Persistent symptoms despite previous conservative treatment * Ability to understand the study information and provide informed consent * Ability to adhere to postoperative follow-up

Exclusion criteria

* Active local or systemic infection * Severe uncontrolled psychiatric illness * Coagulopathy or anticoagulation therapy contraindicating surgery * Pregnancy * Previous extensive surgical interventions on the same site interfering with planned procedure * Inability to comply with follow-up * Any other condition that, in the opinion of the investigator, makes participation unsafe

Design outcomes

Primary

MeasureTime frameDescription
Change in Pain (VAS Score)Baseline, 10-12 days post-op, 3 months post-opChange in pain intensity measured using the visual analogue scale (0-10) to evaluate the clinical effect of surgical intervention.

Countries

Czechia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026