Treating leprosy patients having Erythema Nodosum Leprosum reaction with concurrent Methotrexate and Prednisolone

Not Applicable

• Conditions: Health Condition 1: A303- Borderline leprosy

• Registration Number: CTRI/2020/11/029074
• Lead Sponsor: ondon School of Hygiene and Tropical Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

All of the following six criteria must be met in order for an individual to be eligible (only one of 6A to 6D need to be met):

1. Individuals who diagnosed with leprosy complicated by ENL

2. Individuals with ENL aged 18-60 years old

3. Individuals with ENL deteriorating symptoms

4. Individuals with 10 or more tender, papular or nodular ENL skin lesions

5. Individuals with an EESS score of at least 9

6. Individuals with ENL on:

A. No current anti- ENL treatment

B. Prednisolone up to 30mg per day (if ACUTE) or Prednisolone 10-30mg (inclusive) per day (if RECURRENT/ CHRONIC) or equivalent alternative corticosteroid dose OR

C. Thalidomide or other non-steroidal anti-ENL medication OR

D. A combination of prednisolone (up to 30mg) and another non-steroidal anti-ENL medication (thalidomide, clofazimine, azathioprine, pentoxifylline, ciclosporin, minocycline)

Exclusion Criteria

1) Individuals who were first diagnosed with ENL more than 4 years prior to enrolment

2) Individuals less than 18 years old or older than 60 years

3) Individuals weighing less than 35kg

4) Individuals with 9 or fewer tender, popular or nodular ENL skin lesions

5) Individuals with an EESS score of 8 or less

6) Women of child bearing capacity who decline to use two forms of adequate contraception and men who decline to use two forms of adequate contraception

7) Pregnant or breastfeeding women

8) Individuals with recurrent or chronic ENL who deteriorate on a dose of prednisolone less than 10 mg or more than 30 mg

9)Individuals who have taken methotrexate by any route for the last 12 weeks

10)Individuals with a hypersensitivity to methotrexate or a recognised contraindication ( please see Methotrexate information sheet)

11) Individuals currently diagnosed with Type 1 reaction or Lucioâ??s phenomenon

12) Individuals with the severe abnormalities in screening investigations

13) Positive serology for HIV, Hepatitis B or C

14) Evidence of tuberculosis or pulmonary fibrosis

15) A history of chronic liver disease or excessive alcohol or illicit substance consumption

16) Individuals with severe inter-current infections, uncontrolled diabetes, active peptic ulcer disease, untreated malignancy

17) Individuals unable to attend regularly for assessment or monitoring

Study & Design

• Study Type: Interventional
• Study Design: Not specified