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NCT00059592
Valacyclovir in Immunocompromised Children
Phase 1 trial testing Valacyclovir in Shingles in 37 participants. Completed in 5 May 2005.
30 December 2004
Quick facts
| Lead sponsor | Baylor College of Medicine |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 37 |
| Start date | 7 April 1998 |
| Primary completion | 30 December 2004 |
| Estimated completion | 5 May 2005 |
| Sites | 2 locations across United States |
Drugs / interventions tested
- Valacyclovir — full drug profile →
Conditions studied
- Shingles — all drugs for Shingles →
- Bone Marrow Transplantation — all drugs for Bone Marrow Transplantation →
Sponsor
Baylor College of Medicine
Who can join
Adults 2 to 18, any sex, with Shingles or Bone Marrow Transplantation. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Shingles is an infection commonly seen in children with a weakened immune system (immunocompromised children). The immune system can be weakened as a result of medications that patients receive for cancer or other serious illness or as a result of a bone marrow transplantation. Shingles in children with a weakened immune system may spread throughout the body and in some instances may be life-threatening. Acyclovir is a medication that is routinely used to treat immunocompromised children with shingles in order to prevent further spread of their shingles and to help them heal faster. Acyclovir is also given to bone marrow transplant patients to prevent reactivation of HSV infection. Valacyclovir is a new drug that is metabolized (broken down in the body) to acyclovir. Valacyclovir is given by mouth and studies done in adults have shown it to be more effective than acyclovir given by mouth. The purpose of this study is to * study the pharmacology of this drug (how the body handles this drug), * determine if oral Valacyclovir can be safely given to children with shingles, and * determine the type of side effects that occur when oral Valacyclovir is given to immunocompromised children.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT00059592
- Europe PMC full search
- ASCO Meeting Library
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Other recruiting trials for Shingles
Currently open trials in the same condition.
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Other Baylor College of Medicine trials
Trials by the same sponsor.
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- NCT06834997 — Dronabinol As an Adjunct for Reducing Pain (DARP)-Texas Children's Hospital · Phase 2 · withdrawn
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00059592 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Baylor College of Medicine
- Last refreshed: 4 March 2020
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00059592.
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