- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02430805
Predisposition and Transition Mechanisms From Arterial Hypertension to Heart Failure (Hypercare)
April 27, 2015 updated by: Central Hospital, Nancy, France
Genetics and Genomics of Hypertension Associated With Microinflammation, Oxydative Stress, Chronic Renal Disease and Heart Failure (A2-B2-B3)
This project aims at investigating the genetic, genomic and proteomic basis of hypertension and susceptibility to hypertension-related end organ damage (renal damage and heart failure).
It will include cross sectional as well as follow-up studies with a large number of subjects and variety of phenotypes, to explore the pathophysiology of hypertension and hypertension-related disease.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In all index patients and recruited family members, recorded data will include the following :
- Past medical history, drug history and family history
- Physical examination
- Height, weight, waist and hip circumference
- Cardiac examination
- Vascular examination
- Blood pressure
- Plasma and urine samples
- Body composition (DEXA)
- Tissue Doppler imaging
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Alsace
-
Strasbourg, Alsace, France, 67000
- Centre D'Investigation Clinique de Strasbourg
-
-
Lorraine
-
Nancy, Lorraine, France, 54000
- Hopital Brabois Adulte
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
index patient :
- Caucasian patients of either sex who were diagnosed to have essential hypertension (as defined below) before the age of 50 y.
- The index patient should not be older than 60 years at the time of enrolment.
Definition of hypertension for the index patient:
- If untreated: Systolic blood pressure > 160 mmHg and/or diastolic blood pressure > 95 mmHg.
- If already on treatment: Treatment with more of 2 different antihypertensive drugs at the time of enrolment.
- At least three first degree relatives of whom at least one should be affected and at least one be from a different generation (parents or offspring aged 18 years or above) must be willing to participate in the family study. For definition of hypertension in relatives of the index patient see below.
- Written informed consent
family
- at least three other first degree relatives must be willing to participate in the family study:
- at least one first-degree relative must be affected with diagnosis of hypertension made before age of 50 years AND
- at least one first degree relative must be from a different generation (offspring or parents).
Exclusion Criteria:
index patient :
- Any known form of secondary hypertension, including sleep apnoea syndrome
- Any known previous clinical complications of hypertension (angina, MI, stroke, TIA, peripheral artery disease) at any time
- Any known renal disease, including GFR < 60 mL/min as estimated by the abbreviated MDRD formula, or kidney stones
- Kidney or other organ transplantation
- Type 1 diabetes mellitus
- Heart failure stage D (AHA/ACC criteria)
- Any malignant concomitant diseases or history of malignant diseases within the last five years, with exception of treated squamous skin cancer or basalioma
- Clinical or laboratory signs of acute infection, especially urinary tract infection
- Systemic inflammatory diseases, such as autoimmune diseases, connective tissue diseases or collagenoses.
- Steroids or any other immunosuppressive drug
- Severe known liver disease (ALT or gamma-GT above three-fold of upper normal limit)
- Current alcohol consume of more than 21 drinks/week (1 drink = a bottle (0,33 l) beer, a glass (0,2 l) of wine, or 4 cl = 40 ml of spirit (40%)) or drug abuse such as cocaine
family
- any organ transplantation
- any malignant concomitant disease
- acute infection
- systemic inflammatory disease
- severe liver disease
- current alcohol or drug abuse
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: NOE
multicentric family-based cohort.
prospective and transversal study
|
blood and urine sample
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
genetic biomarkers
Time Frame: time point 1 : first day ; Time point
|
time point 1 : first day ; Time point
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
oxidative stress markers
Time Frame: time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
|
time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
|
|
microinflammation markers
Time Frame: time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
|
time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
|
|
renal function and damage markers
Time Frame: time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
|
time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
|
|
cardiac and large artery growth, remodelling dysfunction and failure markers
Time Frame: time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
|
time point 1 : first day ; Time point 2 : 2 years ; Time point 3 : 4 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: faiez ZANNAD, Pr, Central Hospital, Nancy, France
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2008
Primary Completion (Actual)
February 1, 2015
Study Completion (Actual)
February 1, 2015
Study Registration Dates
First Submitted
February 5, 2010
First Submitted That Met QC Criteria
April 27, 2015
First Posted (Estimate)
April 30, 2015
Study Record Updates
Last Update Posted (Estimate)
April 30, 2015
Last Update Submitted That Met QC Criteria
April 27, 2015
Last Verified
February 1, 2010
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HYPERCARE(english v. 1.0)JRPB3
- Cpp : 07.11.11
- Dgs: 2007-0537
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Hypertension
-
National Taiwan University Hospital Hsin-Chu BranchRecruitingHypertension,Essential | Hypertension, MaskedTaiwan
-
BackBeat Medical IncNot yet recruitingHypertension, Systolic | Hypertension (HTN) | Heart Failure With Preserved Ejection Fraction (HFpEFGeorgia
-
Xuanwu Hospital, BeijingNot yet recruiting
-
Shenzhen Salubris Pharmaceuticals Co., Ltd.Not yet recruiting
-
Instituto de Cardiologia do Rio Grande do SulCompletedHypertension (HTN) | Hypertension ArterialBrazil
-
University of Alabama at BirminghamTroy UniversityCompletedHypertension | Hypertension, Resistant to Conventional Therapy | Uncontrolled Hypertension | Hypertension, White CoatUnited States
-
Franz Rischard, DOAcceleron Pharma, Inc., a wholly-owned subsidiary of Merck & Co., Inc., Rahway...Not yet recruitingPulmonary Hypertension | Pulmonary Arterial Hypertension (PAH)United States
-
Abant Izzet Baysal UniversityNot yet recruitingPRIMARY HYPERTENSIONTurkey (Türkiye)
-
SingHealth PolyclinicsNanyang PolytechnicEnrolling by invitationHypertension,EssentialSingapore
-
Hacettepe UniversityBozok UniversityCompletedHypertension | Arterial Hypertension | Systemic HypertensionTurkey (Türkiye)
Clinical Trials on dna extraction and genotyping
-
University Medical Centre MariborFaculty of Medicine, University of MariborCompletedSelf-Injurious Behavior | Self Injurious Behavior Without Suicidal Intent
-
Marmara UniversityNot yet recruitingMolar-Incisor Hypomineralization
-
Mayo ClinicTerminatedCarcinoma, Squamous Cell | Lung Neoplasms | Lung Cancer | Neoplasms, Lung | Pulmonary Neoplasms | Squamous Cell Carcinoma | Neoplasms, Pulmonary | Pulmonary Cancer | Cancer of Lung | Cancer of the Lung | Carcinoma, SquamousUnited States
-
Nantes University HospitalCompleted
-
Instituto do Cancer do Estado de São PauloFundação de Amparo à Pesquisa do Estado de São PauloCompletedGenetic Predisposition to Disease | Postoperative Nausea | Polymorphism, GeneticBrazil
-
University Hospital "Sestre Milosrdnice"CompletedPeripheral Retinal Degenerations, Age Related Macular Degeneration Polymorphisms
-
Recep Tayyip Erdogan University Training and Research...CompletedLow Caries Experience | High Caries ExperienceTurkey
-
Peking Union Medical College HospitalUnknown
-
Hager ZanatyNot yet recruitingGut Microbiota Dysbiosis in Lupus Nepheritis
-
Hospital Authority, Hong KongChinese University of Hong KongCompleted