Page 1 of Clinical Trials for "Limb Deformities, Congenital", 25 Total Matches
- 1RecruitingLast Updated: May 16, 2012Condition(s): Congenital Abnormalities; Birth Defects; Congenital Defects
- 2CompletedLast Updated: March 3, 2008Condition(s): Fraser Syndrome; Fryns Syndrome; Chromosomal Abnormalities; Abnormalities, Multiple
- 3Active, not recruitingLast Updated: June 24, 2011Condition(s): Marfan Syndrome
- 4RecruitingLast Updated: March 27, 2012Condition(s): Growth Disorder; Mental Retardation; Multiple Abnormalies
- 5Enrolling by invitationLast Updated: June 9, 2009Condition(s): Congenital Vertical Talus; Familial Encephalopathy With Neuroserpin Inclusion Bodies; Idiopathic Generalised Epilepsy; Familial Dementia; X-Linked Mental Retardation
- 6RecruitingLast Updated: April 11, 2012Condition(s): Malformations; Multiple Abnormalies; Polydactyly
- 7Active, not recruitingLast Updated: April 13, 2011Condition(s): Marfan Syndrome
- 8Active, not recruitingLast Updated: August 11, 2010Condition(s): Marfan Syndrome
- 9RecruitingLast Updated: November 15, 2011Condition(s): Unexplained Isolated Provoked Hemorrhages; Familial Bleeding Disorder; Scott Syndrome
- 10RecruitingLast Updated: July 20, 2011Condition(s): Marfan Syndrome
- 11RecruitingLast Updated: March 1, 2012Condition(s): Marfan Syndrome
- 12RecruitingLast Updated: June 8, 2010Condition(s): Marfan Syndrome
- 13CompletedLast Updated: March 3, 2008Condition(s): Connective Tissue Disease; Dissecting Aneurysm; Ehlers Danlos Syndrome; Marfan Syndrome; Nail Patella Syndrome
- 14CompletedLast Updated: February 11, 2011Condition(s): Marfan Syndrome
- 15RecruitingLast Updated: March 31, 2012Condition(s): Coronary Artery Disease; Proteus Syndrome; Coffin - Sins Syndrome; Familial Isolated Hyperparathyroidism; Dubouitz Syndrome
- 16CompletedLast Updated: July 10, 2007Condition(s): Diabetes; Ulceration; Amputation; Foot Deformity; Neuropathy
- 17Active, not recruitingLast Updated: November 9, 2011Condition(s): Marfan Syndrome
- 18RecruitingLast Updated: May 16, 2012Condition(s): Marfan Syndrome; Turner Syndrome; Ehlers-Danlos Syndrome; Loeys-Dietz Syndrome; FBN1, TGFBR1, TGFBR2, ACTA2 or MYH11 Genetic Mutation; Bicuspid Aortic Valve Without Known Family History; Bicuspid Aortic Valve With Family History; Bicuspid Aortic Valve With Coarctation; Familial Thoracic Aortic Aneurysm and Dissections; Shprintzen-Goldberg Syndrome; Other Aneurysms and Dissections of the Thoracic Aorta Not Due to Trauma, <50yo; Other Congenital Heart Disease
- 19CompletedLast Updated: June 12, 2007Condition(s): Marfan Syndrome
- 20Active, not recruitingTriphalangeal Thumbs in the Pediatric Population: Long Term Outcomes Following Surgical InterventionLast Updated: August 25, 2011Condition(s): Phalanx of Supernumerary Digit of Hand
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Limb+Deformities%2C+Congenital%22
