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Use of a Varicella-Zoster Virus (VZV) Vaccine to Prevent Shingles in HIV-Infected Children Who Have Already Had Chickenpox
NCT00001125 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to see if the varicella-zoster virus (VZV) vaccine will be safe and if it can help prevent shingles in HIV-infected children who have already had chickenpox. VZV is the virus that causes chickenpox. If this virus is reactivated in the body, it can also cause shingles. Shingles is common in children with HIV who have had chickenpox, although it is usually not life-threatening. The VZV vaccine used in this study may be able to prevent HIV-positive children who have had chickenpox from developing shingles.
Conditions Studied
Interventions
- BIOLOGICAL Varicella Virus Vaccine (Live)
Study Locations (20)
New York
- Nyu Ny Nichd Crs — New York
- Cornell Univ., Div. of Ped. Infectious Diseases & Immunology — New York
- Columbia IMPAACT CRS — New York
- Harlem Hosp. Ctr. NY NICHD CRS — New York
- Strong Memorial Hospital Rochester NY NICHD CRS — Rochester
- SUNY Upstate Med. Univ., Dept. of Peds. — Syracuse
California
- Long Beach Memorial Med. Ctr., Miller Children's Hosp. — Long Beach
- Usc La Nichd Crs — Los Angeles
- UCLA-Los Angeles/Brazil AIDS Consortium (LABAC) CRS — Los Angeles
- Harbor - UCLA Med. Ctr. - Dept. of Peds., Div. of Infectious Diseases — Torrance
Florida
- South Florida CDTC Ft Lauderdale NICHD CRS — Fort Lauderdale
- Univ. of Florida Jacksonville NICHD CRS — Jacksonville
- Univ. of Miami Ped. Perinatal HIV/AIDS CRS — Miami
Massachusetts
- HMS - Children's Hosp. Boston, Div. of Infectious Diseases — Boston
- BMC, Div. of Ped Infectious Diseases — Boston
- Baystate Health, Baystate Med. Ctr. — Springfield
New Jersey
- Cooper Univ. Hosp. — Camden
- NJ Med. School CRS — Newark
Pennsylvania
- The Children's Hosp. of Philadelphia IMPAACT CRS — Philadelphia
- St. Christopher's Hosp. for Children — Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Est. Completion | 2004-03 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00001125
The ClinicalTrials.gov registry entry for NCT00001125 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Institute of Allergy and Infectious Diseases (NIAID), which has 1,295 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with HIV Infections appearing as the primary indexed condition, and to 1 intervention — of which Varicella Virus Vaccine (Live) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00001125 reports 20 study locations spanning 6 distinct geographic areas — top geographies include New York, California, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00001125 about?
NCT00001125 is a clinical study titled "Use of a Varicella-Zoster Virus (VZV) Vaccine to Prevent Shingles in HIV-Infected Children Who Have Already Had Chickenpox". The purpose of this study is to see if the varicella-zoster virus (VZV) vaccine will be safe and if it can help prevent shingles in HIV-infected children who have already had chickenpox. VZV is the virus that causes chickenpox. If this virus is reactivated in the body, it can also cause shingles. S...
What is the current status of trial NCT00001125?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. Estimated completion is 2004-03.
What conditions does trial NCT00001125 study?
This clinical trial studies the following conditions: HIV Infections, Chickenpox. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00001125?
The interventions under investigation include: Varicella Virus Vaccine (Live) (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00001125?
This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 1,295 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00001125 being conducted?
This trial has 20 study locations across California, Florida, Massachusetts, New Jersey, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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