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Platelet rich plasma in Leprosy neuropathy

An interventional study to assess the effectiveness of single perineural injection of platelet rich plasma on nerve function with special emphasis on nerve function of Hansens disease with truncal (mixed) neuropathy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/046962
Enrollment
30
Registered
2022-11-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: A309- Leprosy, unspecified

Interventions

Intervention1: Autologous Platelet rich Plasma: 1 ml of Freshly prepared autologous Platelet rich plasma given perineurally within 15 minutes of preparation, in patients of Hansens disease with ulnar

Sponsors

AIIMS Bhopal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Known case of Hansen’s disease on or post treatment with Multi drug therapy 2. Age: =18 years 3. Patients of Hansen’s disease with peripheral neuropathy involving Ulnar and/ or Common Peroneal Nerve with residual impairment 4. Willingness to participate in study (informed written consent) 5. Willingness to forego any other concomitant treatment modality

Exclusion criteria

Exclusion criteria: 1. Hansen’s disease diagnosed for more than three years duration. 2. Signs of active inflammation or abscess around the Ulnar or Common Peroneal Nerve 3. Diagnosed case of active lepra reaction 4. Infection at the site of injection 5. Reduced range of motion of knee, elbow, wrist or ankle 6. Abnormal radiograph of elbow joint and knee joint of the affected side 7. Received local steroid injection within 6 months, NSAIDS within one week prior to intervention or on systemic steroids more than 20 mg daily 8. Abnormal haemoglobin or blood count (platelet count , Hb g/dl,Mean platelet volume >12.3 fl) 9. Use of anti-platelet medications 10. Uncontrolled Diabetes Mellitus (FBS >125 mg/dl or PPBS >200 mg/dl) 11. Known case of severe cardiac, liver or renal disease 12. Pregnancy or lactation 13. Unwillingness to participate in study

Design outcomes

Primary

MeasureTime frame
two point discrimination testTimepoint: 0,6, 12 weeks

Secondary

MeasureTime frame
total area of sensory impairment, Nerve conduction study, dynamometry and manual muscle power testing, SALSA scale scoreTimepoint: 0,6, 12 weeks

Countries

India

Contacts

Public ContactAnyesha Saha

AIIMS Bhopal

kothari_sy@yahoo.com9406720172

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026