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Modalities And Safety Of Cardiac Rehabilitation In A Population Managed For Spontaneous Hematoma Or Coronary Disruption

Modalities And Safety Of Cardiac Rehabilitation In A Population Managed For Spontaneous Hematoma Or Coronary Disruption (DISCO): Data From The DISCO Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05744947
Acronym
READAPT-DISCO
Enrollment
90
Registered
2023-02-27
Start date
2023-02-05
Completion date
2023-04-30
Last updated
2023-03-01

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

Conditions

Cardiac Rehabilitation Program Following the Management of ACS in Patients Presenting With SCAD

Keywords

Cardiac rehabilitation, Spontaneous Coronary Artery Dissection

Brief summary

Spontaneous Coronary Artery Dissection (SCAD) is a rare and often misdiagnosed cause of Acute Coronary Syndrome (ACS) affecting predominantly young women without cardiovascular risk factors. There is no definitive evidence on the optimal management of SCAD, but the general approach is conservative. Unlike established evidence-based rehabilitation programs for ACS and heart failure, no cardiac rehabilitation protocol exists for SCAD. The aim of the study is to report and detail the cardiac rehabilitation program which was proposed to patients previously included in The Study of the Prevalence Fibromuscular Dysplasia in Patient With Haematoma or Spontaneous Coronary Artery Dissection. (DISCO trial - NCT02799186).

Detailed description

The cardiac rehabilitation program was proposed to the patients presenting with SCAD in each interventional cardiology department, according physician's in charge of the patient decision. The patient who has undergone a cardiac rehabilitation program following the ACS is included in a retrospective way. The patients are informed about this study by the investigator. After a reflection period, the patient is included. Details regarding the entrance psychosocial evaluation, the entrance exercise treadmill test, the medications changes during rehabilitation, the training program modalities, the exit exercise treadmill test, and the left ventricular ejection fraction evolution (evaluated by echocardiography) were recorded. The safety for each cardiac rehabilitation program was also assessed.

Interventions

OTHERData collection

Specific Readapt -DISCO complementary questionnaire rehabilitation

Sponsors

University Hospital, Bordeaux
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient previously recruited in The Study of the Prevalence Fibromuscular Dysplasia in Patient With Haematoma or Spontaneous Coronary Artery Dissection. (DISCO trial - NCT02799186) : * Patient over 18 years old * Patient with a possible diagnosis of spontaneous coronary dissection defined by: * ACS presentation * Angiographic signs compatible with a SCAD * More or less confirmed by intracoronary imaging (OCT/IVUS) or remote angiographic control (upper to 1 month). * Patient with signed informed consent to participate in the DISCO study * Subject agreeing to the use of his or her personal data in the form of anonymous coding, including in scientific publications. * patient who has undergone cardiac rehabilitation following the management of acute coronary syndrome.

Exclusion criteria

o

Design outcomes

Primary

MeasureTime frameDescription
Safety of the cardiac rehabilitation programday 0 (inclusion)absence/presence of chest pain during cardiac rehabilitation, hospitalization for a cardiac complication during the rehabilitation program

Secondary

MeasureTime frameDescription
Training program modalitiesday 0 (inclusion)Medications changes during cardiac rehabilitation program

Countries

France

Contacts

Primary ContactEdouard GERBAUD, Dr
edouard.gerbaud@chu-bordeaux.fr524 549 188

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026