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Endoscopic Treatment for Isolated, Single Suture Craniosynostosis

This study has been withdrawn prior to enrollment.
(Study was withdrawn due to lack of resources.)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00769847
First Posted: October 9, 2008
Last Update Posted: June 2, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University of Utah
October 7, 2008
October 9, 2008
June 2, 2015
September 2008
July 2009   (Final data collection date for primary outcome measure)
Not Provided
Not Provided
Complete list of historical versions of study NCT00769847 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Endoscopic Treatment for Isolated, Single Suture Craniosynostosis
Endoscopic Treatment for Isolated, Single Suture Craniosynostosis
This is a prospective study to evaluate outcomes in patients undergoing endoscopic craniectomy for isolated, single-suture craniosynostosis.
Not Provided
Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample
Male and female infants, from 1 to 6 months of age with isolated, single-suture sagittal craniosynostosis.
Craniosynostosis
Procedure: Endoscopic strip craniectomy
Surgery
Sagittal synostosis
Male and female infants from 1-6 months of age with isolated, single suture sagittal craniosynostosis.
Intervention: Procedure: Endoscopic strip craniectomy

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
0
September 2013
July 2009   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Infants 1 to 6 months of age with isolated, single-suture craniosynostosis.

Exclusion Criteria:

  • Multiple suture craniosynostosis and infants older than 6 months of age.
Sexes Eligible for Study: All
1 Month to 6 Months   (Child)
Yes
Contact information is only displayed when the study is recruiting subjects
Not Provided
United States
 
NCT00769847
22034
No
Not Provided
Not Provided
Faizi Siddiqi, M.D., Principal Investigator, University of Utah
University of Utah
Not Provided
Principal Investigator: Faizi Siddiqu, MD University of Utah
University of Utah
May 2015