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Impact of Frailty on Immune Response to Varicella-Zoster Vaccination in Community-dwelling Older Adults; Pilot study

Impact of Frailty on Immune Response to Varicella-Zoster Vaccination in Community-dwelling Older Adults; Pilot study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0001807
Enrollment
70
Registered
2016-02-05
Start date
2016-02-22
Completion date
Unknown
Last updated
2020-08-18

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

Conditions

None listed

Interventions

Biological/Vaccine, Non-Stem Cell : One vial (0.65ml) of Zostavax, Varicella-Zoster Virus Vaccine Live (OKA/MERCK), will be injected subcutaneously

Sponsors

Seoul National University Bundang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adults 65 years of age and older. Have given written informed consent prior to enrollment.

Exclusion criteria

Exclusion criteria: No history of herpes zoster within 5 years, no current history of immune suppression (e.g. malignancy or neoplastic disease, corticosteroid therapy). No immunosuppression resulting from disease (e.g. malignancy, HIV infection), corticosteroids (except intermittent topical or inhaled corticosteroid = greater than 800mcg/day beclomethasone dipropionate or equivalent) or other immunosuppressive/cytotoxic therapy (cancer chemotherapy or organ transplantation). No active neoplastic disease (except local skin cancer or prostate cancer that are stable in the absence of immunosuppressive/cytotoxic therapy). No prior receipt of varicella vaccine. No allergic sensitivity to neomycin. No history of anaphylactoid reaction to gelatin. No significant underlying illness that would be expected to prevent completion of the study (e.g., life-threatening disease likely to limit survival to less than 6 months). No receipt of any other immunizations within one month before study vaccination (2 weeks in the case of inactivated influenza vaccines or other non-replicating immunization products) or scheduled within 6 weeks after study vaccination. No currently receiving antiviral therapy. No intercurrent illness (e.g. urinary tract infection, influenza) that might interfere with the interpretation of the study. No subjects unlikely to adhere to protocol follow-up. No subjects involved in a conflicting (vaccine) clinical trial.

Design outcomes

Primary

MeasureTime frame
Difference of immunogenicity will be compared according to the frailty status.

Secondary

MeasureTime frame
Difference of antibody response according to the age group will be assessed.;Difference of immunogenicity will be compared according to the baseline cytokine level.

Countries

Korea, Republic of

Contacts

Public ContactJung-Yeon Choi

Seoul National University Bundang Hospital

Outcome results

None listed

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