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Appendix 6: Data Extraction Form Clinical Review For systematic reviews Reviewer: ___Date: ___Study Characteristics Ref ID: Author(s): Publication title: Publication year: Country (where the study
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How to fill out clinical data extraction form

01
Gather all necessary clinical documents and records related to the patient or study.
02
Identify the specific data fields required in the extraction form based on the study objectives.
03
Carefully read the instructions provided with the clinical data extraction form.
04
Enter patient demographics such as age, gender, and medical history in the designated fields.
05
Record clinical observations, lab results, and vital signs from the clinical documents accurately.
06
If applicable, note any adverse events or complications experienced by the patient.
07
Double-check all entries for accuracy and completeness before submission.
08
Submit the completed form to the designated review board or study coordinator.

Who needs clinical data extraction form?

01
Researchers conducting clinical trials or studies.
02
Healthcare professionals involved in data collection and patient monitoring.
03
Regulatory bodies requiring documentation of clinical data.
04
Companies developing pharmaceuticals or medical devices to gather safety and efficacy data.
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A clinical data extraction form is a standardized document used to collect and report clinical data from various studies or trials, ensuring consistency and accuracy in the collected information.
Typically, clinical researchers, data managers, and investigators involved in clinical trials and studies are required to file the clinical data extraction form.
To fill out a clinical data extraction form, follow the instructions provided, enter accurate data according to the guidelines, and ensure all required fields are completed before submission.
The purpose of the clinical data extraction form is to systematically gather relevant clinical data for analysis, reporting, and ensuring compliance with regulatory requirements.
Information such as patient demographics, treatment details, outcomes, adverse events, and study protocol adherence must be reported on the clinical data extraction form.
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