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Characteristics of Hgb C Carriers in Northern Israel and Clinical Features Among Hgb Homozygous
This study is not yet open for participant recruitment.
Verified by HaEmek Medical Center, Israel, April 2007
Sponsored by: HaEmek Medical Center, Israel
Information provided by: HaEmek Medical Center, Israel
ClinicalTrials.gov Identifier: NCT00481260
  Purpose

Hgb C is an hemoglobinopathy quite rare in Israel. The clinical status of patients that are diagnosed as homozygous to this disease is quite benign but not study in large groups.

Also the characteristics of carriers and the incidence in northern Israel were a large arab population lives, was not study. The results of this study can be useful for screening purpose in a area were another hemoglobinopathies are frequent.


Condition Intervention
Hgb C Hemoglobinopathy
Procedure: Medical history and basic laboratory analysis

U.S. FDA Resources
Study Type: Observational
Study Design: Natural History, Cross-Sectional, Defined Population, Retrospective Study
Official Title: Characteristics of Hgb C Carriers in Northern Israel and Clinical Features Among Hgb Homozygous

Further study details as provided by HaEmek Medical Center, Israel:

Estimated Enrollment: 100
Study Start Date: May 2007
Estimated Study Completion Date: December 2007
Detailed Description:

Hgb C is an hemoglobinopathy quite rare in Israel. The clinical status of patients that are diagnosed as homozygous to this disease is quite benign but not study in large groups.

Also the characteristics of carriers and the incidence in northern Israel were a large arab population lives, was not study. The results of this study can be useful for screening purpose in a area were another hemoglobinopathies are frequent.

The study will record the clinical characteristics of the homozygous Hgb C patients and the hematology characteristics of all the heterozygous carriers detected in northern Israel

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • All patients diagnosed as homozygous for Hgb C disease or double heterozygous in combination to other abnormal hemoglobin, and all the carriers detected in the hematology laboratory during the screening for abnormal hemoglobins in northern Israel
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00481260

Contacts
Contact: Ariel Koren, MD 972-4-6495576 ext 5576 koren_a@clalit.org.il

Locations
Israel
Pediatric Hematology Unit - HaEmek Medical Center
Afula, Israel, 18101
Sponsors and Collaborators
HaEmek Medical Center, Israel
Investigators
Study Director: Ariel Koren, MD Pediatric Hematology Unit, Ha'Emek Medical Center
Study Chair: luci Zalman, Phd Hematology Laboratory - HaeEmek Medical Center
  More Information

Study ID Numbers: 5100706.EMC
Study First Received: May 31, 2007
Last Updated: May 31, 2007
ClinicalTrials.gov Identifier: NCT00481260  
Health Authority: Israel: Ministry of Health

Keywords provided by HaEmek Medical Center, Israel:
Hgb C
Screening

Study placed in the following topic categories:
Genetic Diseases, Inborn
Hematologic Diseases
Hemoglobinopathies
Hemoglobinopathy

ClinicalTrials.gov processed this record on January 16, 2009