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

Results pending

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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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2009-10-31

Study Completion Date

2010-04-30

Brief Summary

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The present study is designed to collect data on real world experience on use of Medrol in acute asthma in Indian patients.

Detailed Description

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Sequential enrollment

Conditions

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Asthma

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Methylprednisolone Group

Oral Methylprednisolone Tablets

Intervention Type DRUG

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

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* To be eligible for enrollment in this study, patients must be prescribed oral Medrol® tablets (4mg and 16 mg) for acute asthma as per the locally approved prescribing information. The prescription of Medrol® will be separated from the decision to include the patient in the study.
* 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

* Based upon history or physical exam in the emergency department (ED) or Clinic, subjects with known or suspected cause of pulmonary symptoms other than asthma, such as COPD, CHF, pneumonia, pulmonary embolism, or angioedema
* Any contraindication to Medrol tablet use. Contraindications of Medrol use are systemic fungal infections and known hypersensitivity to components
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Related Links

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Other Identifiers

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B0121003

Identifier Type: -

Identifier Source: org_study_id

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