Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02721472
Other study ID # DRE-FR-15-1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 17, 2016
Est. completion date November 14, 2019

Study information

Verified date January 2020
Source ADDMEDICA SASA
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the relationship between plasma DNA levels and micro- and macro-circulatory vascular remodelling in patients with sickle cell disease


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date November 14, 2019
Est. primary completion date November 14, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age = 18 years.

- Homozygous SS or Sß0 sickle cell disease patients.

- Seen in consultation for an annual clinical and para-clinical evaluation of his/her disease.

- Stable clinical condition of the disease defined as the absence of severe vaso-occlusive crises (requiring hospitalisation or a visit to the emergency unit) in the previous month and absence of transfusion in the previous 3 months.

Exclusion Criteria:

- Other haemoglobinopathy

- Known diabetes.

- Recent administration of an anticoagulant treatment at curative doses (< 48h before inclusion), or platelet-inhibiting drugs (less than 1 week prior to inclusion).

- Recent transfusion (less than 3 months prior to inclusion).

- Pregnancy or post-partum (first 40 days after giving birth).

- Recent consumption of alcohol (less than 10h), coffee (less than 3h), and tobacco (less than 36h) before inclusion.

- Known infection with hepatitis B, C, and HIV infection.

- Known cancer or progressive blood disease.

- Known haemostasis or coagulation disorders.

- Progressive inflammatory or infectious diseases.

- Recent history (dating less than 3 months) of venous (pulmonary embolism, deep venous thrombosis) or arterial (acute coronary syndrome, stroke, peripheral arterial ischaemia) thromboembolic event.

- Adult patients subject to legal protection measures.

- Patients already involved in a therapeutic protocol.

- Patients not affiliated to a social security system.

- Non-inclusion criteria related to the technical requirements of the Endo-PAT:

- Known cardiac arrhythmia.

- Severe Raynaud's syndrome.

- Hand or arm deformity that prevents an EndoPAT analysis.

Study Design


Intervention

Procedure:
micro- and macro-circulatory vascular remodelling measures not practice in routine care
Vascular measures : reactive hyperaemia index (RHI) assessed by Endo-PAT, central aortic blood pressure, aortic augmentation index, carotid-femoral pulse wave velocity
Biological measures not practice in routine care
Biological measures : Plasma DNA level, NETs (plasma nucleosome levels), Microparticules (MPs) (total, associated with red blood cells, neutrophils, platelets), haem (total and bound to MPs), Myeloperoxydase and elastase activity, neutrophils/DNA, Annexin A5, RNA and TSP1

Locations

Country Name City State
France Hôpital Avicenne Bobigny Ile De France

Sponsors (1)

Lead Sponsor Collaborator
ADDMEDICA SASA

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of plasma DNA levels in patients with a reactive hyperaemia index (RHI) < 1.67 (endothelial dysfunction) assessed by Endo-PAT 2000 versus those recorded in patients with a RHI = 1.67 (no endothelial dysfunction) 1 days
Secondary Relationship between plasma DNA levels and cerebral micro- and macro-angiopathy assessed by CT angiography or MRI angiography and transcranial Doppler ultrasound 1 day
Secondary Relationship between plasma DNA levels and cardiac damages 1 day
Secondary Relationship between plasma DNA levels and pulmonary blood pressure 1 day
Secondary Relationship between plasma DNA levels and macrocirculatory vascular measurements 2 days
Secondary Relationship between plasma DNA levels and nephropathy 1 day
Secondary Relationship between plasma DNA levels and a clinical index of the sickle cell disease severity in a stable condition 1 day
See also
  Status Clinical Trial Phase
Completed NCT02227472 - Working Memory and School Readiness in Preschool-Aged Children With Sickle Cell Disease
Recruiting NCT06301893 - Uganda Sickle Surveillance Study (US-3)
Recruiting NCT04398628 - ATHN Transcends: A Natural History Study of Non-Neoplastic Hematologic Disorders
Completed NCT02522104 - Evaluation of the Impact of Renal Function on the Pharmacokinetics of SIKLOS ® (DARH) Phase 4
Recruiting NCT04688411 - An mHealth Strategy to Improve Medication Adherence in Adolescents With Sickle Cell Disease N/A
Terminated NCT03615924 - Effect of Ticagrelor vs. Placebo in the Reduction of Vaso-occlusive Crises in Pediatric Patients With Sickle Cell Disease Phase 3
Not yet recruiting NCT06300723 - Clinical Study of BRL-101 in Severe SCD N/A
Recruiting NCT03937817 - Collection of Human Biospecimens for Basic and Clinical Research Into Globin Variants
Completed NCT04134299 - To Assess Safety, Tolerability and Physiological Effects on Structure and Function of AXA4010 in Subjects With Sickle Cell Disease N/A
Completed NCT04917783 - Health Literacy - Neurocognitive Screening in Pediatric SCD N/A
Completed NCT02580565 - Prevalence of Problematic Use of Equimolar Mixture of Oxygen and Nitrous Oxide and Analgesics in the Sickle-cell Disease
Recruiting NCT04754711 - Interest of Nutritional Care of Children With Sickle Cell Disease on Bone Mineral Density and Body Composition N/A
Completed NCT04388241 - Preliminary Feasibility and Efficacy of Behavioral Intervention to Reduce Pain-Related Disability in Pediatric SCD N/A
Recruiting NCT05431088 - A Phase 2/3 Study in Adult and Pediatric Participants With SCD Phase 2/Phase 3
Completed NCT01158794 - Genes Influencing Iron Overload State
Recruiting NCT03027258 - Point-of-Delivery Prenatal Test Results Through mHealth to Improve Birth Outcome N/A
Withdrawn NCT02960503 - Macrolide Therapy to Improve Forced Expiratory Volume in 1 Second in Adults With Sickle Cell Disease Phase 1/Phase 2
Completed NCT02567695 - A Single-Dose Relative Bioavailability Study Of GBT440 300 mg Capsules in Healthy Subjects Phase 1
Completed NCT02620488 - A Brief Laboratory-Based Hypnosis Session for Pain in Sickle Cell Disease N/A
Not yet recruiting NCT02525107 - Prevention of Vaso-occlusive Painful Crisis by Using Omega-3 Fatty Acid Supplements Phase 3