Clinical trials

3

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Rosuvastatin for Prevention of Anthracycline-induced Cardiac Dysfunction in Breast Cancer Patients

This study, called "ROSUBREAST", is a multicenter, double-blind, randomized clinical trial evaluating whether rosuvastatin (20 mg daily) can protect the heart in women with breast cancer receiving anthracycline-based chemotherapy. A total of 400 participants will be randomly assigned to receive either rosuvastatin or placebo for 12 months. The main goal is to determine whether rosuvastatin can prevent cancer treatment-related cardiac dysfunction (CTRCD), defined as a significant drop in heart pumping function. The study will also assess changes in cardiac strain, blood biomarkers, symptoms of heart failure, quality of life, and possible side effects.

Participants needed: 400
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: Shiraz University of Medical SciencesUpdated: Dec 10, 2025Locations: 7
Eligibility criteria

Female individuals with ≥18 years of age [+2]

Baseline LVEF < 50% [+9]

Status: Recruiting

CTFFR and Prediction of Non-Significant CAD Lesions

In this prospective cohort study, 250 patients with suspected or known CAD and at least one intermediate coronary lesion (50-70% stenosis) who had a NiFFR value greater than 0.80 underwent coronary computed tomography angiography (CCTA) with NiFFR assessment. Patients were followed for one year to monitor for MACE

Participants needed: 250
Trial details
Age: 20-80Biological sex: AllType: InterventionalSponsor: Shiraz University of Medical SciencesUpdated: May 21, 2025Locations: 1
Eligibility criteria

Patients were enrolled if they had at least one intermediate coronary lesion (cl...

Patients having past coronary artery bypass graft surgery (CABG) [+4]

Status: Recruiting

Ticagrelore Alone Post PCI

After PCI for CCS patients, single center double blind randomization will be done and patients will receive aspirin 80 mg and clopidogrel 75 mg versus 90 mg two times daily of ticagrelor, for 6 months and MACE will be followed in registry of professor Kojuri cardiology clinic

Participants needed: 5,400
Trial details
Phase: Phase 4Age: 20-80Biological sex: AllType: InterventionalSponsor: Shiraz University of Medical SciencesUpdated: May 21, 2025Locations: 2
Eligibility criteria

Male or female above 20 years of age undergoing PCI with a drug-eluting stent fo... [+1]

Contraindication to aspirin, clopidogrel, ticagrelor, or any other reason that s... [+23]