Study of the Efficacy of Losartan on Aortic Dilatation in Patients With Marfan Syndrome (MARFANSARTAN)
Primary Purpose
Marfan Syndrome
Status
Terminated
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
placebo
Losartan
Sponsored by
About this trial
This is an interventional treatment trial for Marfan Syndrome focused on measuring Marfan syndrome, Angiotensin II Type 1 Receptor Blockers, Aortic Aneurysm, Thoracic
Eligibility Criteria
Inclusion Criteria:
- 10 years or older
- Marfan syndrome according to international criteria Signed informed consent
Exclusion Criteria:
- Previous surgery of the ascending aorta, or surgery planned
- Non echogenicity
- Contre-indication lactose
- Pregnancy on going or planned within 3 years
- Breast feeding
- Participation in another clinical study
- Non member of the social security or CMU
Sites / Locations
- Hôpital Bichat
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
A: Placebo
B: Losartan
Arm Description
placebo
Losartan
Outcomes
Primary Outcome Measures
normalised aortic diameter at the level of the sinus of valsalva
Secondary Outcome Measures
cardiac surgery, hospitalisation in cardiology ward, death
Full Information
NCT ID
NCT00763893
First Posted
September 30, 2008
Last Updated
November 3, 2015
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT00763893
Brief Title
Study of the Efficacy of Losartan on Aortic Dilatation in Patients With Marfan Syndrome
Acronym
MARFANSARTAN
Official Title
Multicenter, Randomised, Double Blind Study of the Efficacy of Losartan on Aortic Dilatation in Patients With Marfan Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
October 2015
Overall Recruitment Status
Terminated
Why Stopped
A similar publication has been released, suggesting a beneficial effect of sartans, and only 15 patients remained to be seen for their visit at 36 months.
Study Start Date
September 2008 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
December 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate if losartan limits aortic dilatation in patients with Marfan syndrome.
Detailed Description
Aim : evaluate the efficacy of losartan for limiting aortic dilatation in patients with marfan syndrome receiving standard therapy
Inclusion criteria :
10 years or older Marfan syndrome according to international criteria Signed informed consent
Non inclusion :
Previous surgery of the ascending aorta, or surgery planned Non echogenicity Contre-indication lactose Pregnancy on going or planned within 3 years Breast feeding Participation in another clinical study Non member of the social security or CMU
Number of subjects : the number of subjects (150 per group) is derived from the study from Shores et al (1994) demonstrating the benefit of beta-blockade in Marfan patient and uses a decrease by half of the aortic dilatation with losartan
Follow-up is 3 years, after inclusion period of 2 years. A total of 5 years is expected
Methods : randomised double blind vs placebo study. All French centres de competence for marfan syndrome and the centre de reference are participating in the study.
End points : main endpoint is evolution of normalised aortic diameter. Secondary endpoints include clinical events (cardiac surgery or aortic dissection, hospitalisation in cardiology department, death), tolerance of the drug, and quality of life.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Marfan Syndrome
Keywords
Marfan syndrome, Angiotensin II Type 1 Receptor Blockers, Aortic Aneurysm, Thoracic
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
303 (Actual)
8. Arms, Groups, and Interventions
Arm Title
A: Placebo
Arm Type
Placebo Comparator
Arm Description
placebo
Arm Title
B: Losartan
Arm Type
Active Comparator
Arm Description
Losartan
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
Cover key details of the intervention. Must be sufficiently detailed to distinguish between arms of a study (e.g., comparison of different dosages of drug) and/or among similar interventions (e.g., comparison of multiple implantable cardiac defibrillators). For example, interventions involving drugs may include dosage form, dosage, frequency and duration.
Intervention Type
Drug
Intervention Name(s)
Losartan
Intervention Description
50 mg/day if < weight 50 kg 100 mg/day if weight > 50 kg
Primary Outcome Measure Information:
Title
normalised aortic diameter at the level of the sinus of valsalva
Time Frame
every six months
Secondary Outcome Measure Information:
Title
cardiac surgery, hospitalisation in cardiology ward, death
Time Frame
during the follow up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
10 years or older
Marfan syndrome according to international criteria Signed informed consent
Exclusion Criteria:
Previous surgery of the ascending aorta, or surgery planned
Non echogenicity
Contre-indication lactose
Pregnancy on going or planned within 3 years
Breast feeding
Participation in another clinical study
Non member of the social security or CMU
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guillaume JONDEAU, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Bichat
City
Paris
ZIP/Postal Code
75018
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
20619242
Citation
Detaint D, Aegerter P, Tubach F, Hoffman I, Plauchu H, Dulac Y, Faivre LO, Delrue MA, Collignon P, Odent S, Tchitchinadze M, Bouffard C, Arnoult F, Gautier M, Boileau C, Jondeau G. Rationale and design of a randomized clinical trial (Marfan Sartan) of angiotensin II receptor blocker therapy versus placebo in individuals with Marfan syndrome. Arch Cardiovasc Dis. 2010 May;103(5):317-25. doi: 10.1016/j.acvd.2010.04.008. Epub 2010 Jul 1.
Results Reference
result
PubMed Identifier
25935877
Citation
Milleron O, Arnoult F, Ropers J, Aegerter P, Detaint D, Delorme G, Attias D, Tubach F, Dupuis-Girod S, Plauchu H, Barthelet M, Sassolas F, Pangaud N, Naudion S, Thomas-Chabaneix J, Dulac Y, Edouard T, Wolf JE, Faivre L, Odent S, Basquin A, Habib G, Collignon P, Boileau C, Jondeau G. Marfan Sartan: a randomized, double-blind, placebo-controlled trial. Eur Heart J. 2015 Aug 21;36(32):2160-6. doi: 10.1093/eurheartj/ehv151. Epub 2015 May 2.
Results Reference
result
PubMed Identifier
26052700
Citation
Jiang P, Loyau S, Tchitchinadze M, Ropers J, Jondeau G, Jandrot-Perrus M. Inhibition of Glycoprotein VI Clustering by Collagen as a Mechanism of Inhibiting Collagen-Induced Platelet Responses: The Example of Losartan. PLoS One. 2015 Jun 8;10(6):e0128744. doi: 10.1371/journal.pone.0128744. eCollection 2015.
Results Reference
derived
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Study of the Efficacy of Losartan on Aortic Dilatation in Patients With Marfan Syndrome
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