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Symptomatic Trial of Angina Assessment Prior to Revascularization (ORBITA-STAR)

Imperial College London logo

Imperial College London

Status

Completed

Conditions

Coronary Artery Disease
Angina, Stable

Treatments

Procedure: Percutaneous coronary intervention

Study type

Observational

Funder types

Other

Identifiers

NCT04280575
19HH5060

Details and patient eligibility

About

The principal objective of this research is to determine whether symptoms, induced by confirmed experimental ischaemia, can help us predict which patients will respond to PCI.

Enrollment

80 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Angina or angina-equivalent symptoms
  2. Anatomical evidence of a significant single vessel coronary stenosis on diagnostic coronary angiography indicating ≥ 70% stenosis
  3. Referred for percutaneous coronary intervention for treatment of stable angina

Exclusion criteria

  1. Age younger than 18
  2. Age older than 85
  3. Recent acute coronary syndrome
  4. Multivessel coronary artery disease
  5. Previous coronary artery bypass graft surgery
  6. Significant left main stem coronary disease
  7. Chronic total occlusion in the target vessel
  8. Contraindication to percutaneous coronary intervention or drug-eluting stent implantation
  9. Contraindication to antiplatelet therapy
  10. Contraindication to adenosine infusion
  11. Severe valvular disease
  12. Severe LV systolic impairment
  13. Severe respiratory disease
  14. Life expectancy less than 2 years, pregnancy, unable to consent

Trial contacts and locations

2

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Central trial contact

Christopher A Rajkumar; Rasha K Al-Lamee

Data sourced from clinicaltrials.gov

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