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Comparison of Relapse Rate and Disease Severity among patients with Type 2 Lepra Reaction receiving Tofacitinib and Thalidomide separately as an adjuvant to systemic steroids: A Longitudinal Analytical Study

Comparison of Relapse Rate and Disease Severity among patients with Type 2 Lepra Reaction receiving Tofacitinib and Thalidomide separately as an adjuvant to systemic steroids: A Longitudinal Analytical Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097093
Enrollment
60
Registered
2025-11-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: A305- Lepromatous leprosy

Interventions

Intervention1: Nil: Nil

Sponsors

AIIMS Patna
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: : All patients with Type II lepra reaction age more than 18 years who are attending the Department of Dermatology and receiving Tofacitinib as adjuvant to Prednisolone during the study period. - Patients with Type II lepra reaction age more than 18 years who have received Thalidomide as adjuvant to Prednisolone previously in 2022-23 as available in our department register will also be included in comparison group.

Exclusion criteria

Exclusion criteria: Patients having any active infection or URTI or Diarrhea Immunocompromised status like HIV/Chemotherapy/Radiotherapy Breastfeeding women Severe liver disease or Renal Disease

Design outcomes

Primary

MeasureTime frame
Relapse Rate ENL severity score comparisonTimepoint: At Baseline, 1 month, 3 month and 6 months

Secondary

MeasureTime frame
Adverse events DLQITimepoint: At Baseline, 1 month, 3 month and 6 months

Countries

India

Contacts

Public ContactDr Rishav Sanghai

AIIMS Patna

dr.swetalinapradhan@gmail.com7978843633

Outcome results

None listed

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