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A Survey for Long-term Use of Prograf Capsules in Patient With Interstitial Pneumonia

Completed
Conditions
Interstitial Pneumonia Associated With Polymyositis/Dermatomyositis
Interventions
Registration Number
NCT02159651
Lead Sponsor
Astellas Pharma Inc
Brief Summary

This study is to evaluate the safety and the efficacy of Prograf in patients with interstitial pneumonia associated with polymyositis / dermatomyositis in acute clinical setting.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
179
Inclusion Criteria
  • Hospitalized patient
  • Patient diagnosed with Interstitial pneumonia associated with polymyositis/dermatomyositis
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
2: Polymyositis grouptacrolimuspatients with interstitial pneumonia associated with polymyositis
1: Dermatomyositis grouptacrolimuspatients with interstitial pneumonia associated with dermatomyositis
Primary Outcome Measures
NameTimeMethod
Overall survivalUp to three years
Secondary Outcome Measures
NameTimeMethod
Safety assessed by the incidence of adverse eventsUp to three years

Any adverse events which include adverse events leading to death, white blood cell count, erythrocyte sedimentation rate and other abnormal findings from laboratory tests

Arterial blood gas analysis value (PaO2, AaDO2)Up to three years

Arterial blood gas analysis by PaO2 (arterial O2 pressure) and AaDO2 (alveolar-arterial oxygen difference)

Serum KL-6 value (serum SP-D value)Up to three years

KL-6 (sialylated carbohydrate antigen KL-6) and SP-D (surfactant protein D) are used as marker of interstitial pneumonia

Respiratory function test value (%FVC, %DLco)Up to three years

Respiratory function is evaluated by % FVC ( percent-predicted forced vital capacity) amd %DLco (diffusion capacity of CO).

Chest CT findingsUp to three years

CT: computed tomography

Patient dispositionUp to three years

patient disposition includes 1)number of case report forms collected, 2)number of patients analyzed for safety, 3)number of patients analysed for efficacy

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