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Completed

NCT Number: NCT04177173

Methotrexate and Statins With Methotrexate Alone in the Treatment of Rheumatoid Arthritis

The objective of the study is to compare the efficacy of combination of Methotrexate and Statins with Methotrexate alone in the treatment of Rheumatoid Arthritis. It is hypothesized that adding statins to methotrexate for treatment of rheumatic arthritis will significantly suppress the disease activity as compared to methotrexate alone.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Mayo Hospital

Lahore, Punjab Province, 54000, Pakistan

About this study

After approval from Board of Studies and IRB of King Edward Medical University, all patients fulfilling inclusion and exclusion criteria from out patient department and wards of Mayo Hospital Lahore will be selected and randomized to group A or group B by lottery method (using coin flipping method) with one group receiving combination of methotrexate and simvastatin and other group receiving simvastatin only. All patients will be given adequate dose of analgesics for pain relief. Informed consent will be obtained from the patient. Demographic information like name, age and sex, will also be obtained. DAS 28 scoring will be done at the time of presentation and will be noted. Patients will be followed at 1 month, 3 month and at 6 month. At each follow up DAS 28(ESR) score will be calculated using DAS 28 calculator. All this information will be recorded on predesigned proforma (attached).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients between ages 18 years and above
  • Gender- Both male and female
  • Fulfilling 2010 ACR/EULAR criteria of Rheumatoid arthritis with active inflammatory disease defined by DAS 28 score >2.6,
  • Normal serum cholesterol level.

Exclusion criteria

  • Already diagnosed patients of Diabetes mellitus.
  • Use of steroids greater than 4 weeks of duration or intra articular steroid injection within 4 weeks of study.
  • Statin therapy in last three months.
  • Statin intolerant patient.
  • Elevated Creatinine Phosphokinase more than twice the upper limit of normal range.
  • Diagnosed case of Chronic liver disease or abnormal liver functions (transaminases > 2 times the upper limit of normal range) before the start of treatment or during follow-up.
  • High serum Creatinine level
  • Pregnancy and breast feeding.

Treatment and study plan

Simvastatin 20 mg

Drug

improvement of disease activity

Methotrexate 10 mg

Drug

improvement of disease activity

Primary outcomes

  1. Efficacy of drugs defined by improvement in Disease Activity Score 28 (DAS28)

    Time frame: 6 months

    In Rheumatoid arthritis, DAS28 values range from 2.0 to 10.0 while higher values mean a higher disease activity. A DAS 28 below the value of 2.6 is interpreted as Remission/improvement

Secondary outcomes

  1. Adverse Drug Reaction

    Time frame: 6 months

    Adverse event reported against any of the intervention under study

Sponsors and collaborators

Lead sponsor

King Edward Medical University

Other

Registry information

Official study title

Comparison of Combination of Methotrexate and Statins With Methotrexate Alone as an Anti-inflammatory Agent in the Treatment of Rheumatoid Arthritis.

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Nov 26, 2019
Registry last updated
Nov 26, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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