Overview

Efficacy of Starting Methotrexate Early in Chikungunya Arthritis

Status:
Completed
Trial end date:
2018-05-01
Target enrollment:
0
Participant gender:
All
Summary
This is a single center, prospective, randomized controlled open label trial with a one sided cross over design to compare the efficacy of initiating Methotrexate(Mtx) in early post Chikungunya induced arthritis (4-12 weeks after onset) with Non Steroidal Anti inflammatory Drugs(NSAID) alone.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Postgraduate Institute of Medical Education and Research
Treatments:
Methotrexate
Criteria
Inclusion Criteria:

1. Patients of confirmed CHIK-V infection as per WHO guidelines defined as atleast one of
the following

1. Presence of viral ribonucleic acid in sera determined with RT -PCR in acute phase
< 7 days of fever

2. Presence of virus specific IgM antibodies in serum

2. Persistent arthritis after 4 weeks of onset of fever and duration less than 12 weeks

3. Age more than 16 years

4. Patients willing to give informed consent

Exclusion Criteria:

1. Patients with mixed infection i.e. dengue.

2. Having a known rheumatological disease and currently taking treatment

3. Pregnant and breastfeeding women

4. Any contraindication to methotrexate