Clinical Trials Logo

Cleft Palate clinical trials

View clinical trials related to Cleft Palate.

Filter by:

NCT ID: NCT03839290 Recruiting - Clinical trials for Cleft Lip and Palate

Development of the Palate in Bilateral Orofacial Cleft Newborns One Year After Early Neonatal Cheiloplasty

Start date: September 2016
Phase:
Study type: Observational

Early neonatal cheiloplasty is modified surgery protocol applied in the first week of newborn's life used for treating orofacial cleft patients. This prospective study analyzes the effects of early neonatal cheiloplasty on the growth and development of maxilla and palate during the observed period of one year.

NCT ID: NCT03537976 Recruiting - Cleft Palate Clinical Trials

Targeting Surgeons' Decision-Making for Cleft Lip Surgery

Start date: January 31, 2018
Phase: N/A
Study type: Interventional

Using separate prospective cohorts of patients who have lip revision and lip repair surgery, the objective of this clinical trial is to both qualitatively and quantitatively assess how surgeons integrate the objective measures and visual aids of the Intervention with the systematic subjective assessment in order to determine decisions surgery.

NCT ID: NCT02595307 Recruiting - Clinical trials for Musculoskeletal Diseases

Improving Informed Consent for Cleft Palate Repair

Start date: May 2014
Phase: N/A
Study type: Interventional

To determine if providing a written document in addition to the standard oral discussion of surgical risks improves risk recall for the parents/guardians of a child seen in consultation for cleft palate surgery, and if this has any effect on overall satisfaction after the procedure

NCT ID: NCT01867632 Recruiting - Cleft Palate Clinical Trials

Acellular Dermal Matrix in Primary Furlow Palatoplasty

Start date: September 2012
Phase: N/A
Study type: Observational

The goal of the present study is to definitely determine whether the use of acellular dermal matrix (ADM) during primary cleft palate repair decreases the rate of fistula formation. Although individual studies have described promising advantages to its use in cleft palate surgery, no consensus currently exists. Without concrete evidence, one must question the whether the increased cost, time and potential patient risk (human derived tissue) to patients justifies its use in primary cleft palate repair.

NCT ID: NCT01773278 Recruiting - Hearing Loss Clinical Trials

Cholesterol and Antioxidant Treatment in Patients With Smith-Lemli-Opitz Syndrome (SLOS)

Start date: December 2008
Phase: Phase 2
Study type: Interventional

Patients with biochemically confirmed SLOS are being treated with cholesterol supplementation and antioxidant medication. They are carefully monitored with visits to clinic, laboratory testing including cholesterol and 7-dehydrocholesterol levels, vitamin levels, blood counts and liver and kidney function. On a serial basis, no more often than once a year, the patients undergo a series of tests under anesthesia, including electroretinogram (ERG), brainstem audiometry (ABR), and ophthalmologic exam under anesthesia to follow pigmentary retinopathy.

NCT ID: NCT01601171 Recruiting - Clinical trials for Cleft Lip and Palate

Genetics of Reproductive Disorders (Including Kallmann Syndrome) and Cleft Lip and/or Palate

Start date: March 2012
Phase:
Study type: Observational

The purpose of this study is to explore the genetic basis of reproductive disorders and cleft lip and/or palate.

NCT ID: NCT00285714 Recruiting - Cleft Palate Clinical Trials

3D Imaging of Hard and Soft Tissue in Orthognathic Surgery

Start date: February 2006
Phase: N/A
Study type: Interventional

The primary objective of this clinical trial is to assess the influence of orthognathic surgery on facial soft tissue, such as changes (volume, linear, angular) of facial hard and soft tissue, in three dimensions, so enabling the setup of 3D normative value tables.

NCT ID: NCT00004347 Recruiting - Clinical trials for Smith-Lemli-Opitz Syndrome

Phase II Study of Dietary Cholesterol for Smith-Lemli-Opitz Syndrome

Start date: November 1995
Phase: Phase 2
Study type: Interventional

OBJECTIVES: I. Examine the intestinal absorption of dietary cholesterol in patients with Smith-Lemli-Opitz syndrome. II. Measure the effect of dietary cholesterol on plasma sterol composition. III. Quantify basal cholesterol synthesis, turnover of cholesterol and 7-dehydrocholesterol, and the effects of dietary cholesterol on these parameters. IV. Identify fecal bile acid excretion quantitatively and qualitatively in these patients. V. Compare the incorporation of deuterated water into plasma cholesterol, 7-dehydrocholesterol, and other intermediates, and assess the effect of dietary cholesterol on this incorporation.