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Protocol for tdm
This document outlines a protocol for conducting a therapeutic drug monitoring study, including sections for the title, investigators, study location, patient recruitment details, need for the study, objectives, patient selection criteria, procedures for blood sample collection and storage, instruments for measuring drug and clinical levels, report preparation, clinical interpretation, and conclusion.
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Introduction to the Therapeutic Drug Monitoring protocol presented by Swarna Priya B at Jaya College.
Detailed components of the study protocol including title, investigators, study location, patient recruitment, need, objectives, selection criteria, and methodologies.
Clarification of the study title and the roles of the chief investigator and other personnel involved.
Information on where the study takes place and the sites for patient recruitment.
Importance of Therapeutic Drug Monitoring studies and the objectives aimed at optimizing patient care.
Define selection criteria for participants and the importance of patient history in the study.
Procedures for blood sample withdrawal, storage methods, and instruments used for measuring drug levels and clinical parameters.
The preparation of reports based on the study data and the clinical interpretation of the findings.
Final thoughts and conclusions on the findings and implications of the Therapeutic Drug Monitoring study.
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Protocol for tdm
- 1. PROTOCOL FOR THERAPEUTIC DRUG MONITORING SWARNAPRIYA B JAYA COLLEGE OF PHARMACY, THIRUNINRAVUR, CHENNAI
- 2. PROTOCOL • TITLE OFTHE STUDY/PROJECT • INVESTIGATORS Chief Investigator Joint Investigator Co Investigator – Clinical and Research Fellow • PLACE OF THE STUDY • PATIENT RECRUITMENT PLACE • NEED FOR TDM STUDY • OBJECTIVE OF THE STUDY
- 3. Cont. • CRITERIA FORSELECTION OF PATIENTS • PATIENT HISTORY • WITHDRAWAL OF BLOOD SAMPLE AND STORAGE • INSTRUMENT FOR • Measurement of drug levels • Measurement of clinical parameters (ECG, EEG, RESPIRATION) • REPORT PREPARATION • CLINICAL INTERPRETATION
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- 5. INVESTIGATORS Chief Investigator Joint Investigator CoInvestigator – Clinical and Research Fellow
- 6. PLACE OF THESTUDY
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- 8. NEED FOR TDMSTUDY
- 9. OBJECTIVE OF TDMSTUDY
- 10. CRITERIA OF THESTUDY
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- 12. WITHDRAWAL OF BLOOD SAMPLEAND STORAGE
- 13. INSTRUMENT FOR • Measurementof drug levels • Measurement of clinical parameters (ECG, EEG, RESPIRATION)
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