- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00267345
Measurement of Hormonal Concentration in Chylothorax Fluid in Infants With Congenital Chylothorax
February 28, 2007 updated by: Sheba Medical Center
Late onset Hypothyroidism was found in infant with congenital hypothyroidism.
The hypothesis is that infants with congenital hypothyroidism may lose thyroxin and other hormones via the chylothorax fluid causing transient hypothyroidism.
In this study hormonal concentration will be measured in the chyle as well as hormonal serum level.
Study Overview
Status
Unknown
Conditions
Detailed Description
Late onset Hypothyroidism was found in infant with congenital hypothyroidism.
The hypothesis is that infants with congenital hypothyroidism may lose thyroxin and other hormones via the chylothorax fluid causing transient hypothyroidism.
In this study hormonal concentration will be measured in the chyle as well as hormonal serum level.
Study Type
Observational
Enrollment
15
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jacob Kuint, MD
- Phone Number: 972-3-5302227
- Email: kuint-j@sheba.health.gov.il
Study Locations
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Ramat-Gan, Israel, 52621
- Recruiting
- Sheba Medical Center
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Contact:
- Jacob Kuint, MD
- Phone Number: 972-3-5302227
- Email: kuint-j@sheba.health.gov.il
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Principal Investigator:
- Ayala Maayan, MD
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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
1 hour to 2 months (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Infants with congenital chylothorax requiring thorax drain
Exclusion Criteria:
- none
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
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jacob Kuint, MD, Sheba Medical Center
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
March 1, 2005
Study Completion
October 1, 2007
Study Registration Dates
First Submitted
December 19, 2005
First Submitted That Met QC Criteria
December 19, 2005
First Posted (Estimate)
December 20, 2005
Study Record Updates
Last Update Posted (Estimate)
March 1, 2007
Last Update Submitted That Met QC Criteria
February 28, 2007
Last Verified
January 1, 2006
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SHEBA-05-3927-JK-CTIL
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.
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