Skip to content

Looking at Quick Side Effects of Chemotherapy Treatment Given in One Day at a Cancer Hospital

Analysis of Acute Adverse Drug Reactions Occurring in Day Care Chemotherapy Setting at Tertiary Care Cancer Centre - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/103238
Enrollment
100
Registered
2026-02-06
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C30-C39- Malignant neoplasms of respiratory and intrathoracic organs

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Gopesh Soni
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All Adult (above 18 years) Patients undergoing chemotherapy in the day care setting at the tertiary care cancer centre Patients who provide informed consent for participation in the study

Exclusion criteria

Exclusion criteria: Patients receiving concurrent radiotherapy or immunotherapy in addition to chemotherapy (to avoid confounding due to overlapping toxicities). Patients with known hypersensitivity to any of the chemotherapeutic agents before initiation of treatment. Patients on palliative or end-of-life care, where ADR assessment may be confounded by disease progression. Patients with pre-existing severe organ dysfunction (e.g., hepatic or renal impairment) that could independently predispose to drug toxicity. Patients receiving investigational or unapproved drugs as part of a clinical trial during the study period. Pregnant or lactating women, since chemotherapy safety profiles differ in this population. Patients who leave against medical advice (LAMA) or are lost to follow-up before completion of chemotherapy cycle assessment. Patients with incomplete medical records or missing ADR documentation

Design outcomes

Primary

MeasureTime frame
To determine the incidence of acute drug reactions among patients undergoing chemotherapy in the day care setting. Timepoint: 1 Year

Secondary

MeasureTime frame
To assess the types and patterns of acute adverse drug reactions associated with different chemotherapy regimens. To evaluate the severity of drug reactions using standard grading criteria (WHO-UMC scale) To assess the management strategies for acute drug reactions in the day care chemotherapy setting. Timepoint: 1 Year

Countries

India

Contacts

Public ContactGopesh Soni

Mahatma Gandhi Medical College, Jaipur, Rajasthan

gopeshsoni1@gmail.com8947997300

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026