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Statin and Angiotensin-converting Enzyme Inhibitor on Symptoms in Patients With SCAD (SAFER-SCAD)

Primary Purpose

Coronary Artery Dissection, Spontaneous

Status
Unknown status
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
ramipril
rosuvastatin
placebo
Sponsored by
Cardiology Research UBC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Dissection, Spontaneous focused on measuring Coronary Artery Dissection, Spontaneous, Angina

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Any woman with prior SCAD who is at least 3 months out from her SCAD and has ongoing symptoms of chest pain.
  • Females of child-bearing age must have a negative pregnancy test at enrollment
  • Coronary Flow Reserve(CFR) < 3.0

Exclusion Criteria:

  • Renal dysfunction with Glomerular Filtration Rate <50 ml/min
  • Patients not willing to undergo coronary angiography
  • Patients with a prior intolerance or allergy to rosuvastatin or ramipril
  • Inability to perform CRT or CFR >3.0
  • Obstructive coronary artery disease (stenosis >50% in any artery) or residual dissection >50% with distal flow abnormalities

Sites / Locations

  • Vancouver General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Rosuvastatin, placebo

Ramipril, placebo

Arm Description

rosuvastatin 10-20mg daily or placebo (suggested dose of 10mg for Asians, and 20mg for others)

ramipril (starting dose of ramipril at 5mg daily titrating up to 10mg daily at 1 week if tolerated) versus placebo

Outcomes

Primary Outcome Measures

Angina frequency domain of the SAQ
Angina frequency domain of the SAQ, collected at baseline and after each intervention to assess angina frequency change over time. We hypothesize that mean SAQ will improve by at least 20 points in each treatment group compared to placebo.

Secondary Outcome Measures

Acute coronary syndrome or hospitalization for angina
As a secondary objective, to evaluate whether ACEI or statin versus placebo reduces the combined endpoint of acute coronary syndrome (ACS) or hospitalization for angina at 52 weeks

Full Information

First Posted
December 7, 2013
Last Updated
August 8, 2018
Sponsor
Cardiology Research UBC
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1. Study Identification

Unique Protocol Identification Number
NCT02008786
Brief Title
Statin and Angiotensin-converting Enzyme Inhibitor on Symptoms in Patients With SCAD
Acronym
SAFER-SCAD
Official Title
The Effects of Statin and Angiotensin-converting Enzyme Inhibitor on Coronary Flow Reserve, indEx of Microcirculatory Resistance, and Symptoms in Patients With Spontaneous Coronary Artery Dissection (SAFER-SCAD) Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Unknown status
Study Start Date
June 2014 (undefined)
Primary Completion Date
June 2020 (Anticipated)
Study Completion Date
June 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cardiology Research UBC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
An emerging cause of heart attack in young women is a dissection (or tear) in the coronary arteries. Many of these young women continue to have chest pain long after the tear has healed and this is thought to be due to problems with their small blood vessels of the heart (or microcirculation). We want to determine whether commonly used medications for coronary artery disease including statins (for cholesterol) and angiotensin-converting enzyme inhibitors (for blood pressure) reduce chest pain and improve small vessel function in these patients.
Detailed Description
In patients with spontaneous coronary artery dissection (SCAD), many continue to have ongoing signs and symptoms of ischemia after the dissection has healed. Further, 1 in 5 women will experience recurrent SCAD in long-term follow-up. To date, no study has investigated the pathophysiologic mechanism behind ongoing symptoms or recurrence of SCAD, but microvascular coronary dysfunction (MCD) has been suggested. Coronary reactivity testing (CRT) is an invasive procedure currently being done in MCD patients as the gold standard technique. In particular, a coronary flow reserve (CFR) < 2.5 has been shown to be both diagnostic of the condition and prognostic of a 2 fold increased risk of cardiac events. Please see below for a detailed description of CRT. In brief, a dual temperature and pressure sensor tipped wire by Radi Medical Systems (St Jude Medical, St Paul, MN) will be placed into the dissected and non-dissected coronary arteries of the patient. This will measure CFR by thermodilution and will also allow the measurement of the index of microcirculatory resistance (IMR). IMR has been found to correlate well with true microvascular resistance. In addition to a lack of diagnostic strategies, there is a paucity of research into therapeutic strategies. Most women are conservatively managed with medications, however, there is no consensus as to which pharmacologic therapies should be used. Case reports have suggested benefit with antiplatelet agents (e.g. aspirin) and beta-blockers (reduction of arterial wall shear stress). To date no study has investigated the effects of statins or Angiotensin Converting Enzyme Inhibitors (ACEIs) in SCAD patients. Both agents have been studied in the MCD population and been found to reduce angina frequency and improve CFR after 16 weeks. Purpose: To measuring the CFR and IMR in 40 SCAD patients with ongoing chest pain who are at least 3 months from their dissection to determine the proportion with microvascular dysfunction and to investigate prospectively whether the addition of an ACEI or a statin to usual care in patients with ongoing chest pain and a CFR <3.0 improves chest pain frequency by Seattle Angina Questionnaire (SAQ) at 16 weeks compared to placebo. Hypothesis: We hypothesize that the average CFR in patients at least 3 months out from their SCAD will be <2.5 and that their IMR will be abnormal. Further, we hypothesize that the addition of either an ACEI and/or statin will improve chest pain frequency by at least 20 points on the SAQ at 16 weeks compared to placebo.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Dissection, Spontaneous
Keywords
Coronary Artery Dissection, Spontaneous, Angina

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rosuvastatin, placebo
Arm Type
Experimental
Arm Description
rosuvastatin 10-20mg daily or placebo (suggested dose of 10mg for Asians, and 20mg for others)
Arm Title
Ramipril, placebo
Arm Type
Experimental
Arm Description
ramipril (starting dose of ramipril at 5mg daily titrating up to 10mg daily at 1 week if tolerated) versus placebo
Intervention Type
Drug
Intervention Name(s)
ramipril
Other Intervention Name(s)
Altace
Intervention Description
5-10mg (starting dose 5mg titrating up to 10mg if tolerated after 1 week)
Intervention Type
Drug
Intervention Name(s)
rosuvastatin
Other Intervention Name(s)
crestor
Intervention Description
10-20mg (suggested dose 10mg for Asians, 20mg for everyone else)
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Angina frequency domain of the SAQ
Description
Angina frequency domain of the SAQ, collected at baseline and after each intervention to assess angina frequency change over time. We hypothesize that mean SAQ will improve by at least 20 points in each treatment group compared to placebo.
Time Frame
16 weeks after each intervention
Secondary Outcome Measure Information:
Title
Acute coronary syndrome or hospitalization for angina
Description
As a secondary objective, to evaluate whether ACEI or statin versus placebo reduces the combined endpoint of acute coronary syndrome (ACS) or hospitalization for angina at 52 weeks
Time Frame
1 year

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Any woman with prior SCAD who is at least 3 months out from her SCAD and has ongoing symptoms of chest pain. Females of child-bearing age must have a negative pregnancy test at enrollment Coronary Flow Reserve(CFR) < 3.0 Exclusion Criteria: Renal dysfunction with Glomerular Filtration Rate <50 ml/min Patients not willing to undergo coronary angiography Patients with a prior intolerance or allergy to rosuvastatin or ramipril Inability to perform CRT or CFR >3.0 Obstructive coronary artery disease (stenosis >50% in any artery) or residual dissection >50% with distal flow abnormalities
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tara L Sedlak, MD
Phone
604-875-5487
Email
Tara.Sedlak@vch.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Andrew Starovoytov, MD
Phone
604 875 5079
Email
a.starovoytov@ubc.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tara Sedlak, MD
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vancouver General Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 1M9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tara L Sedlak, MD
Phone
604-875-5487
Email
Tara.Sedlak@vch.ca
First Name & Middle Initial & Last Name & Degree
Jacqueline Saw, MD
First Name & Middle Initial & Last Name & Degree
Tara Sedlak, MD

12. IPD Sharing Statement

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Statin and Angiotensin-converting Enzyme Inhibitor on Symptoms in Patients With SCAD

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