Health Condition 1: C00-D49- Neoplasms
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients willing to provide informed consent 2. both old and new cases 3. patients undergoing radiotherapy, chemotherapy, or palliative treatment 4. life expectancy of at least 4 weeks as assessed by the clinician
Exclusion criteria
Exclusion criteria: 1. Patients not willing to provide written informed consent 2. patients having renal and hepatic dysfunction 3. patients with pre-existing painful comorbidity such as diabetic neuropathy, trigeminal neuralgia, fibromyalgia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in Total Severity Pain Score at Subsequent Visit Will be Taken as Primary Outcome of DrugTimepoint: Baseline (1st visit), 2nd Week | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence, causality, severity, preventability of adverse drug reactions associated with analgesic drugs used in cancer patients during the study period. Timepoint: Baseline (1st visit), 2nd week | — |
Countries
India
Contacts
Government Medical College Haldwani