- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00784173
Middle and Inner Ear Malformation in Children With Velocardiofacial Syndrome
October 31, 2008 updated by: Pontificia Universidade Catolica de Sao Paulo
Middle and inner ear malformations on two boys with velocardiofacial syndrome are discussed.Special attention should be given to the presence of hearing loss due to middle and inner ear malformations, in addition to frequent conductive hearing loss regarding mastoid and middle ear inflammatory processes.
Study Overview
Status
Completed
Detailed Description
Two boys with clinical signs of velocardiofacial syndrome, at ages of 4.7 and 6,7 years old are the subjects of this study.Audiological evaluation, including pure tone audiometry, tympanometry, acoustical reflex, and Computerized Tomography of temporal bones, and analyses of DNA sample with markers of 22q11 region were performed.
Study Type
Observational
Enrollment (Actual)
2
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
Children with velocardiofacial syndrome
Description
Inclusion Criteria:
- Subjects with velocardiofacial syndrome
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.
Investigators
- Principal Investigator: Alfredo Tabith-Junior, MD, Pontificia Universidade Católica de São Paulo
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
January 1, 2007
Primary Completion (Actual)
March 1, 2007
Study Completion (Actual)
June 1, 2007
Study Registration Dates
First Submitted
October 31, 2008
First Submitted That Met QC Criteria
October 31, 2008
First Posted (Estimate)
November 2, 2008
Study Record Updates
Last Update Posted (Estimate)
November 2, 2008
Last Update Submitted That Met QC Criteria
October 31, 2008
Last Verified
October 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Heart Diseases
- Cardiovascular Diseases
- Lymphatic Diseases
- Endocrine System Diseases
- Disease
- Genetic Diseases, Inborn
- Musculoskeletal Diseases
- Parathyroid Diseases
- Heart Defects, Congenital
- Cardiovascular Abnormalities
- Craniofacial Abnormalities
- Musculoskeletal Abnormalities
- Abnormalities, Multiple
- Chromosome Disorders
- 22q11 Deletion Syndrome
- Lymphatic Abnormalities
- Hypoparathyroidism
- Syndrome
- Congenital Abnormalities
- DiGeorge Syndrome
Other Study ID Numbers
- Unique protocol
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.
Clinical Trials on Ear Malformations in the Velocardiofacial Syndrome
-
Karolinska InstitutetErasmus Medical CenterCompletedOsteoarthritis in the Carpometacarpal (CMC) Joint
-
Second Affiliated Hospital, School of Medicine,...RecruitingLocked-In Syndrome;Pulmonary Arteriovenous MalformationChina
-
Regeneron PharmaceuticalsWithdrawnCongenital Hearing Loss Secondary to Biallelic Mutations in the Otoferlin Gene (OTOF) | Biallelic Mutations in the Gap Junction Beta 2 (GJB2) Gene | Digenic Mutations in GJB2/Gap Junction Beta 6 (GJB6) GenesUnited States
-
UNC Lineberger Comprehensive Cancer CenterUNC Translational and Clinical Sciences (Tracs)CompletedA History of Radiation Therapy for a Tumor in the Vicinity of the Retina(s)United States
-
Jazz PharmaceuticalsJazz Pharmaceuticals Research UK LimitedTerminatedSeizure in Participants With Tuberous Sclerosis Complex | Seizure in Participants With Dravet Syndrome | Seizure in Participants With Lennox-Gastaut SyndromeUnited States, Spain, Italy
-
Transposon Therapeutics, Inc.TerminatedAicardi-Goutières Syndrome (AGS)France, Italy, United Kingdom
-
Assistance Publique - Hôpitaux de ParisUnité de Recherche Clinique Necker Cochin, FranceCompleted
-
Children's Hospital of PhiladelphiaEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsWithdrawnAicardi Goutières SyndromeUnited States
-
University of EdinburghMedical Research Council; NHS LothianCompletedAicardi-Goutières SyndromeUnited Kingdom
-
IRCCS Fondazione Stella MarisCompletedAicardi-Goutières Syndrome (AGS)Italy