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Effect of Cabergoline on rheumatiod Arthritis patient

Effect of Cabergoline on rheumatiod Arthritis patient

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138802061828N2
Enrollment
10
Registered
2009-06-29
Start date
2009-05-22
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. Other seropositive rheumatoid arthritis

Interventions

Intervention 1: First group: Cabergoline (1mgr/week) for 3 months and after one month as wash out period, we will change drug to placebo. Intervention 2: Second group: Placebo (once weekly) for 3 mon
Treatment - Drugs
First group: Cabergoline (1mgr/week) for 3 months and after one month as wash out period, we will change drug to placebo
Second group: Placebo (once weekly) for 3 months and after one month as wash out period, we will change placebo to cabergoline (1mgr/week)

Sponsors

Mazandaran University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: patient with Rheumatoid Arthritis (RA) based on ACR (american college of romahthology) 1987 criteria and activity of RA will be defined as existence of 4 swollen joints and two of these : 6 tender joints, morning stiffness>30 minutes and ESR=28. Patients should be received DMARDs (diseases modifying slow acting anti rheumatiod drugs) at least for 3-6 months before entry to study. Exclusion criteria includes: patient uncompromised, psychological problems, pregnancy and lactation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The number of tender joints. Timepoint: before prevention and 3,4 and 7 month after prevention. Method of measurement: taking history and Questionnaire.;Morning stiffness. Timepoint: before prevention and 3,4 and 7 month after prevention. Method of measurement: taking history and Questionnaire.;The number of swollen joints. Timepoint: before prevention and 3,4 and 7 month after prevention. Method of measurement: examination.;Pain. Timepoint: before prevention and 3,4 and 7 month after prevention. Method of measurement: VAS.

Secondary

MeasureTime frame
ESR. Timepoint: before intervention and 3,4 and 7 mounth after treatment. Method of measurement: labratory.;Prolactine. Timepoint: before intervention and 3,4 and 7 mounth after treatment. Method of measurement: labratory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMotahareh Kheradmand

Mazandaran Univercity of medical sciences and Health ervices

elhamkheradmand2003@yahoo.comkheradmand@mazums.ac.ir+98 15132612458

Outcome results

None listed

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