A Study To Assess The Safety And Effectiveness Of Medrol® In Acute Asthma In Indian Patients
NCT ID: NCT00971893
Last Updated: 2018-11-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2009-10-31
2010-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Methylprednisolone Group
Oral Methylprednisolone Tablets
Oral Methylprednisolone tablets given as per locally approved prescribing information
Interventions
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Oral Methylprednisolone Tablets
Oral Methylprednisolone tablets given as per locally approved prescribing information
Eligibility Criteria
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Inclusion Criteria
* Medrol® tablets, will be prescribed to the patient by the physician according to his/her usual practice. The decision to prescribe Medrol® tablet will necessarily precede and will be independent of the decision to enroll patient into the study. Only those patients who have been prescribed Medrol® tablets will be evaluated for their potential eligibility for the study
* Only those patients, who are ready and willing to sign an informed consent, will be included in the study
* Subject can be contacted through telephone
Exclusion Criteria
* Any contraindication to Medrol tablet use. Contraindications of Medrol use are systemic fungal infections and known hypersensitivity to components
ALL
No
Sponsors
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Pfizer
INDUSTRY
Responsible Party
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Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Related Links
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To obtain contact information for a study center near you, click here.
Other Identifiers
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B0121003
Identifier Type: -
Identifier Source: org_study_id
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