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Safety and Efficacy of Oral and Intravenous Angipars in Patients with Coronary Artery Disease Unsuitable for Heart Surgery or Percutaneous Intervention.

Safety and Efficacy of Oral and Intravenous Angipars in Patients with Coronary Artery Disease Unsuitable for Heart Surgery or Percutaneous Intervention.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138902063799N1
Enrollment
30
Registered
2010-05-13
Start date
2011-08-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic coronary artery disease. Atherosclertic heart disease

Interventions

Intervention 1: Oral Angipars (1 Cap/BD) for 12 weeks as well as Intravenous Angipars (Infusion of 1 Amp/week) for 12 weeks. Intervention 2: Intravenous Angipars (Infusion of 1 Amp/week) for 12 weeks
Treatment - Drugs
Oral Angipars (1 Cap/BD) for 12 weeks as well as Intravenous Angipars (Infusion of 1 Amp/week) for 12 weeks
Intravenous Angipars (Infusion of 1 Amp/week) for 12 weeks / No Control

Sponsors

Pars Roos Company
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1- Proven Coronary Artery Disease (CAD) 2- Unsuitable for Coronary Artery Bypass Graft (CABG) or Percutaneous Intervention (PCI) 3- Ejection Fraction (EF) < %40 Exclusion Criteria: 1- Simultaneous valvular disease (moderate or severe) 2- Debilitating or severe co-morbidity (neurological impairment, respiratory or renal or liver diseases or cancers) 3- Enrolment in another Clinical Trail in previous 3 month 4- non-compliance 5- Severe or unstable clinical feathers 6- Overt heart failure

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical and Paraclinical Signs and Symptoms of Cardiac Ischemia. Timepoint: Every week for 12 weeks. Method of measurement: Past Medical History, Physical Examination, Functional Class and Life Style, Biochemical Tests, EKG, Perfusion Scan, Stress Echocardiography and .

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Rezaei

Cardiac Transplantation Research Center (CTRC)

ctrc@tums.ac.ir; mh_rezaei@yahoo.om+98 21 8863 3037

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026