1.
Subcommittee should consist of:
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Convenor
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President ISCCM (ex officio)
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Secretary ISCCM (ex officio)
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Convenor – Certicifate course(ex officio)
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Member – adult section
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Member – adult section
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Extra member – for first 2 years
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Extra member – for first 2 years
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Member – pediatric section
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Member – pediatric section
3.
Procedure for conduction a specific study
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Identify central coordinator for the specific study
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Prepare / submit a formal p0rotocol, including data analysis plan
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Protocol to be peer-reviewed by a “Protocol Review committee” of ISCCM
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Will identify studies to be conducted
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Suggest modifications to improve study design, protocol
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Recommendations will be sent to central study coordinator for incorporation
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Identify centers who wish to participate in the study
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Select centers to participate in study
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Identify persons who are responsible for data analysis.
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Identify who are going to be authors – names and sequence
Suggest – central study coordinator, 2-3 others involved in planning, conduct
and analysis + 2-3 of centers contributing maximum number of patients / data
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Approval of “Ethics Committee of all study centers
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Conduct of study
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End of study – data cleaning up, analysis
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Prepare report for circulation to participating centers, research subcommittee
and Protocol Review Committee that had initially reviewed the protocol
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Present abstract at an appropriate conference
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Publication
President
ISCCM R
K Mani
Secretary
ISCCM C
K Jani