Expired Study
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Palo Alto, California 94303


Purpose:

To provide oral ganciclovir to patients who require maintenance for control of cytomegalovirus (CMV) retinitis, but who lack patent permanent central venous access for long-term administration of intravenous drugs.


Study summary:

Patients receive oral ganciclovir as maintenance. Patients enrolled at time of closure of enrollment will receive 2 months of study drug and undergo follow-up.


Criteria:

Inclusion Criteria Patients must have: - AIDS. - Stable CMV retinitis. - Treatment with IV ganciclovir or IV foscarnet for at least 18 of the past 21 days. - No permanent central IV catheter at present. - Had a permanent central IV catheter removed two or more times within the past 6 months due to catheter infection or thrombosis. - Consent of guardian if less than legal age of consent. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: - Require continuation of concomitant medications precluded by this protocol. Concurrent Medication: Excluded: - Intravitreal anti-CMV treatment. - Any other concomitant medications precluded by the protocol. Patients with the following prior condition are excluded: History of hypersensitivity to acyclovir or ganciclovir.


NCT ID:

NCT00002135


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Palo Alto, California 94303
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: September 21, 2017

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