World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 27 June 2016
Main ID:  NCT00617721
Date of registration: 05/02/2008
Prospective Registration: Yes
Primary sponsor: University Hospital, Strasbourg, France
Public title: Markers of Defective Membrane Remodelling in Scott-like Syndromes
Scientific title: Defect in Cell Stimulation and Unexplained hemorrhagesMarkers Related to Membrane Remodelling in the Prognosis Scott-like Syndormes
Date of first enrolment: June 2008
Target sample size: 29
Recruitment status: Terminated
URL:  https://clinicaltrials.gov/show/NCT00617721
Study type:  Observational
Study design:  Observational Model: Family-Based, Time Perspective: Prospective  
Phase:  N/A
Countries of recruitment
France Martinique
Contacts
Name:     Lélia GRUNEBAUM, MD
Address: 
Telephone:
Email:
Affiliation:  Hôpitaux Universitaires de Strasbourg
Key inclusion & exclusion criteria

Inclusion Criteria:

- Patients with unexplained provoked hemorrhages (surgery, tooth extraction, birth …),
and associated with reduced prothrombin consomption (residual prothrombine in serum >
à 5%).

- Family members of the patients defined above, with or without unexplained hemorrhages
(symptomatic or not).

- Patient's approval based on detailed information given by the pratician

Exclusion Criteria:

- Patients with primary hemostasis defect or defective blood coagulation factor(s)
possibly explaining the bleeding disorder.

- Anémia,

- patients known to be affected by Factor V New York .

- Patients enrolled in a previous clinical study, the exclusion period of which is not
yet completed. - Collaboration to the study rejected by the patient

- Patients that are not registered for medical care social insurance.



Age minimum: 2 Years
Age maximum: 80 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Unexplained Isolated Provoked Hemorrhages
Familial Bleeding Disorder
Scott Syndrome
Intervention(s)
Other: Blood withdrawal
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
3930
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Aventis, Génopôle d'Evry.
Institut National de la Santé Et de la Recherche Médicale, France
Louis Pasteur University, Strasbourg
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history