Skip to content

Recovery of Sensation, Movement and Pain Relief After Nerve Surgery in Patients with Traumatic Brachial Plexus Palsy

Correlation between sensorimotor recovery and pain relief in patients operated for post traumatic brachial plexus palsy a prospective observational study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/06/112428
Enrollment
25
Registered
2026-06-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: G540- Brachial plexus disorders

Interventions

Intervention1: Nil: Nil

Sponsors

KASTURBA MEDICAL COLLEGE AND KASTURBA HOSPTAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 18 to 65 years with post-traumatic brachial plexus palsy undergoing surgical reconstruction in the form of nerve grafting and/or nerve transfer, having neuropathic pain with DN4 score greater than or equal to 4, and willing to participate with written informed consent

Exclusion criteria

Exclusion criteria: Patients aged below 18 years or above 65 years, those in whom primary exploration and nerve grafting or nerve transfer is not indicated, those with coexisting musculoskeletal conditions, and patients unwilling to participate or unable to comply with scheduled follow-up visits.

Design outcomes

Primary

MeasureTime frame
Neuropathic pain will be assessed using the Douleur Neuropathique 4 (DN4) Questionnaire and Neuropathic Pain Symptom Inventory (NPSI). Motor recovery will be evaluated using the Medical Research Council (MRC) Muscle Grading System, active range of motion (AROM), and grip and pinch strength. Sensory recovery will be assessed using two-point discrimination (2PD) and the Semmes Weinstein Monofilament Test.Timepoint: pre-operatively and at 3, 6, 9, and 12 months post-operatively.

Secondary

MeasureTime frame
Patient-reported functional outcome will be assessed using the Brachial Assessment Tool (BrAT)Timepoint: pre-operatively and at 3, 6, 9, and 12 months post-operatively

Countries

India

Contacts

Public ContactL CHARAN KUMAR REDDY

KASTURBA MEDICAL COLLEGE AND KASTURBA HOSPITAL

anm.acharya@manipal.edu8217736961

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026