Terminé

ITP0207Randomized Study of the Treatment of Primary Immune Thrombocytopenic Purpura (ITP) in Newly Diagnosed Untreated Adult Patients. Comparison of Standard Dose Prednisone Versus High-dose Dexamethasone.

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Ce qui est testé

dexamethasone

+ quality-of-life assessment

+ prednisone

MédicamentProcédure
Qui peut participer

Cytopénie+15

+ Maladies Auto-immunes

+ Troubles de la coagulation sanguine

De 18 à 80 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Étude thérapeutique

Phase 3
Interventionnel
Date de début : avril 2008
Voir le détail du protocole

Résumé

Sponsor principalGruppo Italiano Malattie EMatologiche dell'Adulto
Dernière mise à jour : 27 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Date de début de l'étude : 1 avril 2008

Date à laquelle le premier participant a commencé l'étude.

OBJECTIVES: Primary * To evaluate the role of therapy intensification in adult patients with newly diagnosed, previously untreated primary immune thrombocytopenic purpura with high-dose dexamethasone (HD-DXM), in terms of improvement of response at 6 months after initial response, in comparison with standard-doses of prednisone. Secondary * Compare rate of initial response. * Compare quality of response. * Compare rate of final responses and rate of persistent response. * Compare rate of bleeding events. * Determine rate of resumed response with HD-DXM in non-responder patients or patients who have lost response (arm I only). * Compare time to platelet number increase until a hemostatically effective level is reached and/or disappearance of bleeding symptoms. * Compare rate of rescue interventions. * Compare rate of eligible patients for splenectomy. * Compare rate of patients who underwent splenectomy. * Compare rate of patients who develop connective tissue diseases or underlying hematological diseases (myelodysplastic syndromes, chronic lymphoproliferative diseases, others). * Compare patient's self reported quality of life. OUTLINE: This is a multicenter study. Patients are stratified by treating center. Patients are randomized to 1 of 2 treatment arms. * Arm I (Standard-dose prednisone): Patients receive oral prednisone at a standard dose (1 mg/Kg) once daily on days 1-28 followed by a 14-day taper. Patients considered non-responders at day 42 or who have lost response before evaluation of final response (day 180) are crossed to arm II. * Arm II (High-dose dexamethasone): Patients receive oral dexamethasone at a high dose (40 mg/day) once daily on days 1-4. Treatment repeats every 14 days for 3 courses. Quality of life is assessed at baseline, on day 42 (arm I) or 46 (arm II) (initial response evaluation day), 180 days after initial response evaluation, and at 3, 9, 12 months after randomization. After completion of study treatment, patients are followed monthly until 1 year after randomization, every 2 months for 1 year, and then every 3 months for 1 year.

Titre officielRandomized Study of the Treatment of Primary Immune Thrombocytopenic Purpura (ITP) in Newly Diagnosed Untreated Adult Patients. Comparison of Standard Dose Prednisone Versus High-dose Dexamethasone.
NCT00657410
Sponsor principalGruppo Italiano Malattie EMatologiche dell'Adulto
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

150 participants à inclure

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

Traitement

Cette étude teste un ou plusieurs traitements pour évaluer leur efficacité contre une maladie ou un problème de santé spécifique. L'objectif est de voir si un nouveau médicament ou une thérapie fonctionne mieux, ou provoque moins d'effets secondaires que les options existantes.



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.

De 18 à 80 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

CytopénieMaladies Auto-immunesTroubles de la coagulation sanguineTroubles des Plaquettes SanguinesMaladies HématologiquesMaladies hématologiques et lymphatiquesHémorragieTroubles hémorragiquesMaladies du Système ImmunitaireProcessus pathologiquesPurpura thrombocytopéniquePurpuraSignes et symptômesManifestations cutanéesConditions pathologiques, signes et symptômesThrombocytopéniePurpura thrombopénique idiopathiqueMicroangiopathies Thrombotiques

Critères

Inclusion criteria * Signed written informed consent according to IGH/EU/GCP and national local laws * Newly diagnosed untreated ITP adult patients * Age \> 18 \< 80 years * Platelet count \<20x109/L * Platelet count \> 20 x109/L and \<50x109/L plus bleeding with score \> 8 (according to grading scale at paragraph 7.1) * Baseline Quality of Life evaluation questionnaire filled in Newly diagnosed untreated ITP adult patients * Age \> 18 \< 80 years * Platelet count \<20x109/L * Platelet count \> 20 x109/L and \<50x109/L plus bleeding with score \> 8 (according to grading scale at paragraph 7.1) * Baseline Quality of Life evaluation questionnaire filled in Exclusion criteria * Active malignancy at time of study entry * Steroids administration (PDN \<1mg/Kg/day) for more than 5 days before randomization * Concomitant treatment with anti-platelet and or anti-coagulant drugs * Concomitant severe psychiatric disorders * Not confirmed diagnosis of ITP for * \*Positivity of autoimmunity markers: antinucleus (≥1:80), anti-tireoglobulin, anti-tireoperoxidase, anti-cardiolipin (≥ 40 GPL UmL), anti-b2glycoprotein (≥ 40 IgG U/mL) antibodies, Lupus Anticoagulant (KCT ratio, dRVVT ratios ≥1.5 times the upper normal limit ), direct antiglobulin test (DAT ). * Presence of autoimmune hemolytic anemia * Presence of connective tissue disease * Women who are pregnant or breastfeeding * Cardiovascular diseases requiring treatment * Severe non-controlled, despite therapy, hypertension and diabetes * Liver and kidney function impairment (creatinine, ALT, AST \>2 times upper normal limit) * HCVAb, HIVAb, HBsAg, HBcAb seropositive status * Chronic liver disease * Documented viral illness by the positivity of IgM, or vaccination both occurred one month before diagnosis * Intake of drugs not previously taken within one week before diagnosis * Bleeding score 15 due to ICH or to GI bleeding (according to grading scale at paragraph 7.1, Tab. 3) * Active gastric ulcer.

Plan de l'étude

Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.
Groupes de traitement
Objectifs de l'étude

2 groupes d'intervention sont désignés dans cette étude

Cette étude ne comporte pas de groupe placebo. 

Groupes de traitement

Groupe I

Expérimental
DXM is administered orally at single fixed daily doses of 40 mg for 4 consecutive days, every 14 days, for 3 consecutive courses. If platelet count is £ 20x109/L or bleeding symptoms related to thrombocytopenia are present, lowdose DXM (0.035 mg/Kg/day) between courses is given. The patients (either from ARM A+B or from ARM B) considered NOT RESPONDER at day 46 or who HAVE LOST THE RESPONSE within the evaluation of final response (see paragraph 8.1), will be considered OFF TREATMENT. For these patients a second line therapy will be considered, according to the medical practice of the Centre (splenectomy or other).

Groupe II

Expérimental
PDN is administered orally at the daily dose of 1 mg/Kg for 4 consecutive weeks (from day 0 to day 28), then, therapy is tapered within 14 days. The patients considered NOT RESPONDER at day 42 or WHO HAVE LOST THE RESPONSE within the evaluation of final response (see paragraph 8.1), will be crossed to ARM B.

Objectifs de l'étude

Objectifs principaux

Objectifs secondaires

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 42 sites

Suspendu

U.O. di Ematologia - Azienda Ospedaliera - Pia Fondazione di Culto e di Religione Card. G.Panico

Tricase, ItalyOuvrir U.O. di Ematologia - Azienda Ospedaliera - Pia Fondazione di Culto e di Religione Card. G.Panico dans Google Maps
Suspendu

S.O.C. di Ematologia - Azienda Ospedaliera - SS. Antonio e Biagio e Cesare Arrigo

Alessandria, Italy
Suspendu

Azienda ospedaliera Nuovo Ospedale "Torrette"

Ancona, Italy
Suspendu

USL 8 - Ospedale S.Donato

Arezzo, Italy
Terminé42 Centres d'Étude