Radial Artery Patency and Clinical Outcomes Trial

NCT ID: NCT00475488

Last Updated: 2022-05-27

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 605 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 1996-06-30
• Study Completion Date: 2023-12-31

Brief Summary

Coronary Artery Bypass Graft (CABG)Surgery is commonly used to treat patients with coronary artery disease (atherosclerosis) for the relief of angina (chest pain) and improve heart muscle function.

Healthy veins or arteries, referred to as 'conduits' from elsewhere in the patient's body, are grafted (attached) from the aorta to the coronary arteries, bypassing (via new routes) coronary artery narrowings caused by atherosclerosis (hardening of the arteries) and thereby improving the blood supply to the myocardium (heart muscle).

Over the years, a range of different veins and arteries from around the body have been used to bypass diseased coronary arteries. Typically, internal thoracic arteries from behind the breastbone and the saphenous veins from the legs are used for bypass. More recently, radial arteries from the forearm have also been used to bypass coronary arteries that are diseased (atherosclerotic). There is strong evidence to indicate that the left internal thoracic artery stays open the longest (i.e. has the highest patency) and achieves the best health outcomes. As a result, most cardiac surgeons use the left internal thoracic artery as their first choice of conduit (vessel used to bypass the blocked artery). However, many patients require multiple grafts and there is little evidence as to which grafts are the best conduits to use.

It has been suggested that the radial arteries might function better than saphenous veins as conduits. The Radial Artery Patency and Clinical Outcomes Trial(RAPCO) aims to compare patency of the radial arteries with the right internal thoracic artery and also with the saphenous vein.

Detailed Description

The Department of Cardiac Surgery at Austin Health is conducting a prospective randomised trial, stratified into two separate sub-studies. The first compares the radial artery with the right internal thoracic artery(as a free aorto-coronary graft) and the second comparies the radial artery with a saphenous vein graft. Each patient was to be followed for 10 years after their CABG surgery in order to assess both the pattern of graft survival over 10 years and also to record major clinical events.

The study was first given approval by the Austin Health Human Research Ethics Committee on August 18th,1995. Enrolment commenced in June 1996. Recruitment ceased in March 2005. Patients were randomly assigned to the control or experimental group, patients in both groups received the left internal thoracic artery to the left anterior decending(LAD) and the study graft as the second graft.

The gold standard measure for the comparison of conduits is through the use of post-operative angiograms. These angiograms assess how patent (open) the grafts are, and also offer quality assurance of the CABG surgery performed. To spread the graft patency end-points over the 10 years after CABG, patients undergo a second randomisation as to the time at which their graft patency is to be assessed. The timing of the graft study coronary angiogram is weighted towards the end of the 10 year period with the aim of having 10% at 1 year, 20% at 2 years, 20% at 5 years, 30% at 7.5 years and 30% at 10 years after CABG surgery. Clinical data is systematically collected to determine those patients who experience heart attack, repeat surgery, balloon angioplasty or death over subsequent years.

To enrich the number of mid-study graft patency end-points a protocol amendment(July 19th, 2002) was approved allowing patients to be offered a selective coronary angiogram at the 5 year anniversary of their surgery.

A further protocol amendment(November 16th, 2006) allowed coronary and graft CT angiography to be used optionally to replace selective angiography and also to offer all patients imaging at 10 years, in addition to the original pre-specified, randomised time of imaging.

As per the ethics approval and prior protocol amendments, lifelong followup is conducted on patients enrolled in the trial. As such, a RAPCO-Extension trial will be conducted, evaluating clinical outcomes at 15-years follow-up.

Conditions

Coronary Artery Disease; Atherosclerosis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Group 1

Radial Artery versus Right Internal Thoracic Artery when used as a coronary conduit in patients undergoing multi-vessel coronary artery bypass grafting.

Group Type: OTHER

Coronary artery bypass grafting

Intervention Type: PROCEDURE

Surgery performed due to coronary artery disease.

Group 2

Radial Artery versus Saphenous Vein when used as a coronary conduit in patients undergoing multi-vessel coronary artery bypass grafting.

Group Type: OTHER

Coronary artery bypass grafting

Intervention Type: PROCEDURE

Surgery performed due to coronary artery disease.

Interventions

Coronary artery bypass grafting

Surgery performed due to coronary artery disease.

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• The patient is scheduled for primary coronary artery bypass surgery alone ie. no reoperations, no associated procedures
• The patient requires more than 1 graft, that is, there are at least 2 coronary artery stenoses of > 70%.

Exclusion Criteria

• Renal disease with a creatinine >0.30 mmol/L.
• Chronic heart failure (NYHA Class III or IV or ejection fraction <35% on angiography or radionuclide ventriculography).
• Associated major illnesses e.g., malignancy.
• Body mass index (BMI) > 35; weight (kg)/height(m2).
• Acute presentation, that is, those patients who have an acute myocardial infarct within one week prior to surgery or who present with cardiogenic shock.
• Technical exclusions e.g. sequential grafting.
• Failure to obtain informed consent.
• Off pump.

GROUP 1 Specific exclusions

• Failure to use radial artery due to abnormal Allen Test (>10 sec)
• Failure to be able to use the FRIMA eg. Chest trauma
• FEV1 < 50% of expected value
• Diabetic patients (IDDM or NIDDM) ≥60 years
• Patients ≥70 years

GROUP 2

• Specific exclusions
• Failure to use radial artery due to abnormal Allen Test (>10 sec)
• Failure to be able to use the saphenous vein eg. Varices, past trauma
• Diabetic patients <60 years of age
• Other patients <70 years of age

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Austin Health

OTHER_GOV

Sponsor Role: lead

Responsible Party

David L Hare

Professor David L Hare

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

David L Hare, MB BS DPM FRACP FESC FACC

Role: STUDY_DIRECTOR

Austin Health

Locations

Austin Health

Melbourne, Victoria, Australia

Countries

Australia

References

Buxton BF, Hayward PA, Raman J, Moten SC, Rosalion A, Gordon I, Seevanayagam S, Matalanis G, Benedetto U, Gaudino M, Hare DL; RAPCO Investigators*. Long-Term Results of the RAPCO Trials. Circulation. 2020 Oct 6;142(14):1330-1338. doi: 10.1161/CIRCULATIONAHA.119.045427. Epub 2020 Oct 5.

Reference Type: DERIVED

PMID: 33017209 (View on PubMed)

Other Identifiers

V1111-1166-3083

Identifier Type: OTHER

Identifier Source: secondary_id

H2006/02690

Identifier Type: -

Identifier Source: org_study_id