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Sponsored by: |
University Hospital, Clermont-Ferrand |
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Information provided by: | University Hospital, Clermont-Ferrand |
ClinicalTrials.gov Identifier: | NCT00751452 |
determine the interest of the dosage of citrullinemia to monitor the bowel damage after allogeneic bone marrow transplantation in children.
Condition |
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Benign Disease |
Study Type: | Observational |
Study Design: | Prospective |
Official Title: | Evaluation of Citrullinemia as a Marker of Bowel Damage After Allogeneic Bone Marrow Transplantation in Children |
Estimated Enrollment: | 30 |
Study Start Date: | April 2008 |
Estimated Study Completion Date: | September 2009 |
Estimated Primary Completion Date: | September 2009 (Final data collection date for primary outcome measure) |
Groups/Cohorts |
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1 |
2 |
30 children included. Dosage of citrullinemia on day -7, day 0 and every week up to 100 days after BMT. Histological examination and extensive infectious screening in case of persistent digestive symptoms (more than 3 days).
Two groups of patients regarding on digestive involvement. Comparison of the values of citrullinemia between these two groups.
Ages Eligible for Study: | up to 18 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
screening
Inclusion Criteria:
Exclusion Criteria:
Contact: Lacarin Patrick | placarin@chu-clermontferrand.fr |
France | |
Etienne MERLIN | Recruiting |
Clermont-Ferrand, France, 63003 |
Principal Investigator: | Merlin Etienne, Dr | University Hospital, Clermont-Ferrand |
Responsible Party: | CHU Clermont-Ferrand ( Merlin Etienne ) |
Study ID Numbers: | CHU-0040 |
Study First Received: | September 9, 2008 |
Last Updated: | September 26, 2008 |
ClinicalTrials.gov Identifier: | NCT00751452 |
Health Authority: | France: Ministry of Health |
Children Allogeneic bone marrow transplantation Intestinal damage |
Citrulline Graft versus Host Disease 0 to 18 years old |
Metabolic Diseases Amino Acid Metabolism, Inborn Errors Graft versus host disease Central Nervous System Diseases Brain Diseases Homologous wasting disease Metabolism, Inborn Errors Inborn amino acid metabolism disorder |
Genetic Diseases, Inborn Graft vs Host Disease Brain Diseases, Metabolic, Inborn Metabolic disorder Citrullinemia Brain Diseases, Metabolic Argininosuccinate synthetase deficiency |
Nervous System Diseases |