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A study to evaluate prescription pattern and monitorining of side effects related with drugs prescribed in patients with Rheumatoid Arthritis

Prescription pattern and adverse drug reactions monitoring in Rheumatoid arthritis patients of tertiary care hospital.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2010/091/000550
Enrollment
200
Registered
2010-06-09
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- patients of Rheumatoid arthritis Health Condition 2: M069- Rheumatoid arthritis, unspecified

Interventions

Intervention1: Noting down prescription details and eliciting ADR details, Survey: question based survey Control Intervention1: NIL: NIL

Sponsors

Maulana Azad Medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients with diagnosis of Rheumatoid arthritis and on treatment for at least 6 months with minimum of 2 contact periods will be included in the study. American College of Rheumatology revised criteria for the diagnosis and classification of RA will be adopted for diagnosis

Exclusion criteria

Exclusion criteria: Newly diagnosed patients of Rheumatoid arthritis

Design outcomes

Primary

MeasureTime frame
number of drugs prescribed per prescription,cost of drug,drugs prescribed form EDL,drugs precribed with generic/brand name,Usage of complemetary alternative medicine,Type of ADR encounteredTimepoint: At enrollment—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactDr Bhupinder kalra

Maulana Azad Medical College

drbskalra@gmail.com9968604487

Outcome results

None listed

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