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Pamidronate and disease activity in rheumatoid arthritis

Evaluatoin of intravenous pamidronate effect on disease activity in patients with rheumatoid arthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138801051778N1
Enrollment
37
Registered
2010-04-06
Start date
2009-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Rheumatoid arthritis. Seropositive rheumatoid arthritis

Interventions

Infusion of 60 mg Pamidronate intravenously each month for three months.
Treatment - Drugs
Infusion of 60 mg Pamidronate intravenously each month for three months

Sponsors

Vice chancellery of research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Rheumatoid arthritis patients who don’t have enough clinical and laboratory response to conventional disease modifying anti rheumatic drugs (DMARDs). Exclusion criteria: patients who don’t want to have injection or had drug allergy or hypersensitivity, Drug reaction in the course of injection or after that, Lapse from study, Immigration or death.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Disease activity. Timepoint: Before of injection, every month until 3 months, then 6 months after first injection. Method of measurement: DAS28.

Secondary

MeasureTime frame
Anti inflammatory effect of pamidronate. Timepoint: Before of injection, every month until 3 months, then 6 months after first injection. Method of measurement: DAS28, ESR, VAS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMansour Salesi

Isfahan University of Medical Sciences

salesi@med.mui.ac.ir+98 31 1265 1983

Outcome results

None listed

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