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Observational study to see how long the SARS CoV-2 virus remains alive in the nose and throat of cancer patients on chemotherapy

A Prospective observational study to establish the duration of persistence of replication-competent SARS-CoV-2 in oncology patients with COVID-19 on chemotherapy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/04/033068
Enrollment
50
Registered
2021-04-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere Health Condition 2: C00-D49- Neoplasms

Interventions

Intervention1: Not applicable: Not applicable Control Intervention1: Not applicable: Not applicable

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Oncology patients admitted with RT-PCR confirmed COVID-19 illness 2. Age 1 to 80 years 3. Patients willing to consent for additional blood and nasopharyngeal swabs.

Exclusion criteria

Exclusion criteria: 1. ICU patients unable to give nasopharyngeal swab or blood sample for study proposes 2. Patients with other inter-current bacterial viral respiratory infections. 3. Patients in palliative therapy

Design outcomes

Primary

MeasureTime frame
Determine the duration of persistence of replication-competent/infectious virus in oncology patients.Timepoint: At the baseline and at the time repeat nasopharyngeal swab if required as per standard reassessment

Secondary

MeasureTime frame
1. To establish correlation between RT-PCR (Ct value) and persistence of replication competent SARS-CoV-2Timepoint: At the baseline and at the time repeat nasopharyngeal swab if required as per standard reassessment;2. To identify cancer specific and chemotherapy regimen related risk factors for persistence of replication-competent virusTimepoint: At the baseline and at the time repeat nasopharyngeal swab if required as per standard reassessment;To evaluate whether specific cancer diagnoses or regimens of chemotherapy influence the occurrence of mutation in immune dominant regions in SARS-CoV-2 isolates from oncology patientsTimepoint: At the baseline and at the time repeat nasopharyngeal swab if required as per standard reassessment and during the chemotherapy as per the standards;To identify biomarkers (blood parameters like lymphocyte count neutrophil to lymphocyte ratio, inflammatory markers, viral serology) to predict clearance of replication-competent virus in oncology patients on chemotherapyTimepoint: At the baseline and at the time repeat nasopharyngeal swab if required as per standard reassessment;To identify presence of replication-competent virus in oncology patients who demonstrate a positive RT-PCR after two consecutive negative results(Re-infection)Timepoint: At the baseline and at the time repeat nasopharyngeal swab if required as per standard reassessment

Countries

India

Contacts

Public ContactDr Chetan Dhamne

Tata Memorial Hospital

chetandhamne@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026