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临床试验/CTRI/2021/01/030675
CTRI/2021/01/030675尚未招募4 期

An ambispective cohort study to assess the efficacy of immunosuppressive therapy in systemic sclerosis associated interstitial lung disease.

All India Institute of Medical Sciences0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Patients with a diagnosis of systemic sclerosis as per the 2013 American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) classification criteria, irrespective of their gender, will be included in the study. They may have either diffuse cutaneous or limited cutaneous systemic sclerosis.
  • 2. Age >=18 years.
  • 3. Patients with the following evidence of pulmonary involvement:
  • a)% predicted FVC less than or equal to 70% and/ or
  • b)HRCT chest showing involvement of more than or equal to 20% of lung area with interstitial lung disease
  • 4.Patients already on immunosupressives, who have a baseline and a follow-up PFT and HRCT available

排除标准

  • 1. Patients with overlap syndrome.
  • 2. Diagnosis of clinically significant resting pulmonary hypertension requiring treatment diagnosed on echocardiography (defined as tricuspid regurgitation velocity more than 4m/s, equivalent to estimated pulmonary artery systolic pressure of 64 mm Hg) while evaluation of the patient during study.
  • 3. Evidence of uncontrolled congestive heart failure, unstable ischemic heart disease, history of pulmonary embolism, or cardiac arrhythmia requiring chronic anticoagulation.
  • 4. FVC less than or equal to 15% at baseline.
  • 5. More than 50% area of lung showing fibrosis on HRCT chest at baseline.
  • 6. Hematologic abnormality at screening including:
  • a) Leukopenia (white blood cells [WBC] < 4.0x103/µl).
  • b) Thrombocytopenia (platelet count < 150.0x103/µl).
  • c) clinically significant anemia (hemoglobin < 7 g/dl).
  • d) Participants with an identified and correctable etiology will be eligible if repeat testing shows values greater than the above mentioned cut-off.
  • 7. A diagnosis of chronic liver disease or abnormal baseline liver function tests (total bilirubin or liver enzymes, alanine aminotransferase and aspartate aminotransferase > 2.0 times the upper normal limit).
  • 8. Serum creatinine >2.0mg/dl
  • 9. Pregnancy and/or breast feeding
  • 10. If of child bearing potential (a female participant less than 55 years of age who has not been postmenopausal for more than 5 years or who has not had a hysterectomy and/or oophorectomy), failure to employ reliable means of contraception.
  • 11. Prior use of oral or intravenous cyclophosphamide, MMF, azathioprine or other putative disease modifying medications in last 3 months (assessed at baseline).
  • 12. Current use, or use within the 30 days prior to their baseline visit, of prednisone (or equivalent) in dose of 40 mg/day
  • 13. Active infection (Hepatitis B, Hepatitis C, tuberculosis, HIV) whose management would be compromised by immunosuppression.

研究者

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