An observational study to evaluate drug utilization pattern and adverse drug reaction profile in radiotherapy and oncology section.
Phase 4
- Conditions
- Health Condition 1: null- Adverse drug reaction profile and drug utilization pattern in radiotherapy and oncology section.
- Registration Number
- CTRI/2016/11/007421
- Lead Sponsor
- Department of Pharmacology Government Medical College Bhavnagar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
1.All the participants undergoing chemotherapy in day care centre during the study time period will be enrolled.
2.All participants receiving anti-cancer regimens, will be included in the study .
ï?§3.Participants of any age group
Exclusion Criteria
Patients not receiving any kind of cancer chemotherapy
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method â?¢To analyze drug utilization pattern. <br/ ><br>â?¢To identify the ADRâ??s caused by anti-cancer drugs <br/ ><br>Timepoint: In morning OPD hours and in evening round ( 3days per week)for 2 year duration.
- Secondary Outcome Measures
Name Time Method <br/ ><br>â?¢Information of patient like name, age, gender, weight, and address of patient. <br/ ><br>â?¢Information of drug, its dose, dosage form, mode of administration and total duration of therapy. <br/ ><br>â?¢Treatment according to STG( Standard treatment guidelines) or not. <br/ ><br>â?¢To determine ADRs due to multidrug anticancer regimens <br/ ><br>and to evaluate its causality , severity, preventability, <br/ ><br>whether it is reversible or irreversible and to study drug utilization pattern in cancer patients. <br/ ><br>Timepoint: In morning OPD hours and in evening round ( 3days per week)for 2 year duration.