Allopurinol in Patients With Refractory Angina to Improve Ischemic Symptoms (ARAMIS)
A Single-center, Randomized, Double-blind, Placebo-controlled Study of the Efficacy and Safety of Allopurinol in Improving Ischemic Symptoms in Patients With Refractory Angina.
Sponsor: Fundação de Amparo à Pesquisa do Estado de São Paulo
This PHASE2/PHASE3 trial investigates Refractory Angina and is currently ongoing. Fundação de Amparo à Pesquisa do Estado de São Paulo leads this study, which shows 8 recorded versions since 2021 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
8 versions recorded-
Sep 2025 — Present [monthly]
Unknown PHASE2/PHASE3
-
Sep 2024 — Sep 2025 [monthly]
Unknown PHASE2/PHASE3
-
Jul 2024 — Sep 2024 [monthly]
Unknown PHASE2/PHASE3
Status: Unknown Status → Unknown · Phase: PHASE2_PHASE3 → PHASE2/PHASE3
-
Mar 2023 — Jul 2024 [monthly]
Unknown Status PHASE2_PHASE3
Status: Recruiting → Unknown Status
-
Mar 2021 — Mar 2023 [monthly]
Recruiting PHASE2_PHASE3
Status: Enrolling By Invitation → Recruiting
▶ Show 3 earlier versions
-
Jan 2021 — Mar 2021 [monthly]
Enrolling By Invitation PHASE2_PHASE3
-
Jun 2020 — Jan 2021 [monthly]
Enrolling By Invitation PHASE2_PHASE3
-
May 2020 — Jun 2020 [monthly]
Enrolling By Invitation PHASE2_PHASE3
First recorded
Eligibility Summary
No eligibility information available.
Contact Information
- Fundação de Amparo à Pesquisa do Estado de São Paulo
- InCor Heart Institute
- Ministry of Health, Brazil
For direct contact, visit the study record on ClinicalTrials.gov .