Terminé

Discontinuation of Maintenance Therapy for Cytomegalovirus (CMV) Retinitis After Immune Reconstitution by Potent Antiretroviral Therapy: Safety, Virology, and Immunology Profiles

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Ce qui est collecté

Collecte de données

Qui peut participer

Infections transmises par le sang+24

+ Maladies génito-urinaires

+ Maladies Génitales

À partir de 13 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Observationnel
Voir le détail du protocole

Résumé

Sponsor principalNational Institute of Allergy and Infectious Diseases (NIAID)
Dernière mise à jour : 27 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

This study proposes to assess the hypothesis that, in HIV-infected patients with treated and healed CMV retinitis, an increase in CD4+ T-cells after initiation of potent antiretroviral therapy is either directly related to, or a marker of, immunologic protection for CMV retinitis and is associated with a recovery in specific proliferation responses to CMV antigens. In this study, 100 patients \[AS PER AMENDMENT 7/2/99: 50 patients\] with treated and healed, non-immediate sight-threatening CMV retinitis will discontinue maintenance therapy for suppression of CMV retinitis. Patients are studied in 2 groups. Patients enrolled in Group 1 have CD4+ counts greater than 100 cells/mm3. Group 2 patients have CD4+ counts of 50-100 cells/mm3 and a minimum of a 2 log10 decrease in plasma HIV-1 RNA level or plasma HIV-1 RNA levels below the limit of detection while receiving potent antiretroviral therapy for at least 8 weeks prior to entry \[AS PER AMENDMENT 7/2/99: Group 2 has been withdrawn\]. An additional 25 patients who meet eligibility requirements but who choose to continue to receive maintenance therapy may also participate. All patients are followed to evaluate the relationship between reactivation or progression of CMV disease and changes in CMV DNA, HIV-1 RNA, and CD4+ cell counts. Patients are seen at Weeks 2, 4, 6 and 8, and every 4 weeks until study closure or for 12 months after the last subject is enrolled. \[AS PER AMENDMENT 12/24/98: Patients with confirmed moderate to severe "immune recovery vitritis" should receive a 3-week course of systemic steroids (oral prednisone recommended). Moderate immune recovery vitritis is defined as symptomatic decrease in visual acuity of 2 or more Snellen lines along with, in the absence of active CMV disease, either 2+ or greater vitreous haze as defined by Nussenblatt et al., or cystoid macular edema.\] \[AS PER AMENDMENT 7/2/99: During the course of the study in patients with confirmed cystoid macular edema and a concomitant reduction in visual activity below 20/40, both attributable to immune recovery vitritis/uveitis only, a 21-day course of oral prednisone is recommended. This initial course of steroids helps to determine whether there is an improvement in vision or a decrease in macular edema. Long-term management of immune recovery vitritis/uveitis may include intraocular injection of steroids. Ophthalmoscopic examinations and laboratory tests are performed as per protocol.\]

Titre officielDiscontinuation of Maintenance Therapy for Cytomegalovirus (CMV) Retinitis After Immune Reconstitution by Potent Antiretroviral Therapy: Safety, Virology, and Immunology Profiles
NCT00000905
Sponsor principalNational Institute of Allergy and Infectious Diseases (NIAID)
Dernière mise à jour : 27 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design

75 participants à inclure

Nombre total de participants que l'essai clinique vise à recruter.

Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères

Tout sexe

Le sexe biologique des participants éligibles à s'inscrire.

À partir de 13 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains non autorisés

Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.

Conditions

Pathologie

Infections transmises par le sangMaladies génito-urinairesMaladies GénitalesMaladies TransmissiblesInfections à cytomégalovirusInfections par virus ADNMaladies oculairesInfections à HerpèsviridaeSyndromes de Déficience ImmunologiqueMaladies du Système ImmunitaireInfectionsProcessus pathologiquesMaladies de la rétineRétiniteInfections à RetroviridaeInfections à virus ARNMaladies Sexuellement TransmissiblesConditions pathologiques, signes et symptômesMaladies viralesMaladies Sexuellement Transmissibles ViralesInfections à VIHInfections oculairesInfections oculaires viralesInfections à LentivirusRétinite à cytomégalovirusÉvolution de la maladieAttributs de la maladie

Critères

Inclusion Criteria You may be eligible for this study if you: * Are HIV-positive. * Have a CD4 count greater than 100 cells/mm3. * Have healed CMV retinitis after receiving anti-CMV therapy for at least 8 weeks within 3 months prior to study entry. * Have taken antiretroviral therapy for at least 8 weeks prior to study entry; combination therapy must include at least 2 of the following: protease inhibitors (PIs), nucleoside reverse transcriptase inhibitors (NRTIs), or non-nucleoside reverse transcriptase inhibitors (NNRTIs). * Have a life expectancy of at least 6 months. * Are at least 13 years old (need consent if under 18). Exclusion Criteria You will not be eligible for this study if you: * Have any unstable or severe medical conditions that would keep you from completing the study. * Require chemotherapy or radiation therapy. * Have a history of certain eye disorders.

Centres d'étude

Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.

Cette étude comporte 25 sites

Suspendu

Univ of Southern California / LA County USC Med Ctr

Los Angeles, United StatesOuvrir Univ of Southern California / LA County USC Med Ctr dans Google Maps
Suspendu

UCLA CARE Ctr

Los Angeles, United States
Suspendu

Willow Clinic

Menlo Park, United States
Suspendu

Univ of California / San Diego Treatment Ctr

San Diego, United States
Terminé25 Centres d'Étude