Title o the study:
Title of the sheet:
You are invited to participate in the clinical research study.
Why the study needs to be conducted?
What actually will be done in the study?
How long study may take? How much time I need o take out for study?
Why am I being requested to participate in study?
Are there any benefits of participation?
How many such subjects will be in the study?
What are risks/ inconvenience ilvolvwd?
What will the cost of participation?
Will my results be informed to me?
Is my participation compulsory?
Will by details be available to any general public?
Can I withdraw from study?
How does my participation remain confidential?
Who will take care of mishaps during the study and its expenses?
Is similar study is approved in the hospital going on?
Who should I contact for more information or complaints?
1. Principal investigator
2. co investigators
3. Ethics committee secretary and contact number?
I here declare that I have read through the informed consent document and understood in details. I have no confusion abot study procedures and I consent voluntarily as a participant for said clinical study.
Title of the sheet:
You are invited to participate in the clinical research study.
Why the study needs to be conducted?
What actually will be done in the study?
How long study may take? How much time I need o take out for study?
Why am I being requested to participate in study?
Are there any benefits of participation?
How many such subjects will be in the study?
What are risks/ inconvenience ilvolvwd?
What will the cost of participation?
Will my results be informed to me?
Is my participation compulsory?
Will by details be available to any general public?
Can I withdraw from study?
How does my participation remain confidential?
Who will take care of mishaps during the study and its expenses?
Is similar study is approved in the hospital going on?
Who should I contact for more information or complaints?
1. Principal investigator
2. co investigators
3. Ethics committee secretary and contact number?
I here declare that I have read through the informed consent document and understood in details. I have no confusion abot study procedures and I consent voluntarily as a participant for said clinical study.
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