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Investigation of the Effectiveness of CoronaVac Vaccine in Cancer Patients With Active Chemotherapy and Comparison With Healthy People.

Investigation of the Effectiveness of CoronaVac Vaccine in Cancer Patients With Active Chemotherapy and Comparison With Healthy People.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04765215
Enrollment
291
Registered
2021-02-21
Start date
2021-03-31
Completion date
2022-03-31
Last updated
2021-06-11

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

Conditions

Is the Coronovac Vaccine Effective in Patients Receiving Chemotherapy

Keywords

coronovac, covid-19

Brief summary

This study aimed to investigate the effectiveness of CoronaVac vaccine, which is more than 90% protective in healthy people, in cancer patients receiving active chemotherapy. In this study, to collect information to measure the amount of antibodies produced by the vaccine in the blood of volunteers with the CoronoVac vaccine and to compare it with healthy volunteers.

Interventions

BIOLOGICALCoronoVAC

SARS-CoV-2 IgM and IgG will be measured from blood samples between 3-6 weeks after the 2nd dose of vaccination

Sponsors

Asoc. Prof. Erdoğan Selçuk Şeber
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* Group 1 1. 18 years old and above 2. Having completed two doses of CoronoVac vaccine on time 3. Those with a pathological diagnosis of breast cancer or lung cancer 4. Being the first dose of vaccine during active chemotherapy period 5. Ecog performance score 0-1 6. Patients who signed the informed voluntary consent form * Group 2 1. Over 18 years old 2. Ecog performance score is 0-1 3. Those who have completed 2 doses of coronovac vaccine within the recommended period 4. Volunteer who signed the informed consent form

Exclusion criteria

* For all groups 1. Being confirmed or suspected covid-19 before vaccination 2. Symptomatic covid-19 infection 3. Being addicted to alcohol or drugs 4. Having a fever of 37.8 ° C as a suspect before vaccination 5. Aspleni

Design outcomes

Primary

MeasureTime frameDescription
Antibody levels above the defined cut-offBetween the third and sixth weeks after the second dose of vaccineSARS-CoV-2 IgG II ≥ 50.0 AU/ml (positive) and SARSCoV- 2 IgM \>1 (positive)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026