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Cleft Palate clinical trials

View clinical trials related to Cleft Palate.

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NCT ID: NCT02415361 Completed - Cleft Palate Clinical Trials

Follow Ups of Parents With Infants With Cleft Lip and Palate

Start date: April 2015
Phase: N/A
Study type: Interventional

In Norway, 100-120 children are born with CLP (1.9 per 1,000 live births) each year. Parents of infants with CLP need information and support, especially with feeding immediately after birth. These needs are often not met. The purpose of this study is to investigate the effect of systematic follow ups of parents with infants with CLP performed by a special trained nurse. Parental information needs, parental coping and stress and infant growth and feeding will be explored and compared to a control group receiving standard care. 26 parents (mothers and fathers) or more shall be included in each group according to specific criteria. The control should be examined first. Both groups will answer questionnaires 3 times during the child's first year.

NCT ID: NCT02350803 Completed - Cleft Palate Clinical Trials

Does Use of Rigid Fixation After Removing Distraction Osteogenesis Device Reduce the Relapse?

Start date: February 2011
Phase: Phase 2
Study type: Interventional

patients were enrolled by the inclusion criteria and were undergo lefort 1 maxillary osteotomy. after the latency phase the distraction was done in anterior- posterior vector. patients were divided by randomized allocation in 2 groups. in group 1 the distractor was removed after consolation phase, and in group 2 fixation devices were placed immediately after removal of distractors. data regarding relapse were analyzed by lateral cephalogram X-ray taken in 3 different phases of the trial. change of occlusal plane and the "A point" of the cephalometric analysis were determined as reference point of the study.

NCT ID: NCT02329509 Completed - Cleft Palate Clinical Trials

Evaluation of Facial Growth in Two Primary Protocols Used in the Surgical Treatment of Unilateral Cleft Lip and Palate Patients

Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate which surgical protocol for treating Unilateral Cleft Lip and Palate (UCLP), a single or two stage repair ( with hard palate late closure) will have less impact in mid facial growth. The study hypothesis states that a two stage cleft palate repair , with a late hard palate repair will reduce maxillary growth impairment.

NCT ID: NCT02247193 Completed - Cleft Palate Clinical Trials

Botulinum Toxin to Improve Cosmesis of Primary Cleft Lip Repair

Start date: December 2015
Phase: Phase 1/Phase 2
Study type: Interventional

Objective: To determine if the use of botulinum toxin during primary cleft lip repair improves the cosmetic appearance of the cleft lip scar

NCT ID: NCT01820689 Completed - Clinical trials for Bilateral Complete Cleft Lip and/or Alveolus

Tympanometric Analysis in Cleft Palate

Start date: January 2012
Phase: N/A
Study type: Interventional

Purpose: Characterize the profile of tympanometric patients with cleft lip and palate in the post surgery period and correlate it with the time of palatoplasty. Methods: The sample consisted of 16 patients with cleft lip or palate totaling 32 ears treated at a Public University Hospital in Cuiabá (MT)- Brazil, in the post surgery moment that varied from three months to 33 years. Were sampled patients of both sexes, pediatrics and adults.

NCT ID: NCT01616953 Completed - Trauma Clinical Trials

Cell Therapy for Craniofacial Bone Defects

Start date: August 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this research is to determine if a patient's own bone marrow tissue can help regenerate bone in the area of the jaw where an implant will be placed. The name of the process is called Bone Repair Cell (BRC) Therapy. A sample of bone marrow tissue will be collected and sent to a laboratory where it will be processed to form more cells. These new cells will then be transplanted in the regenerative site. The researchers are testing to see if these cells (BRC) will help form bone. The research will also determine if the implant will be more stable in the area with new bone growth.

NCT ID: NCT01535131 Completed - Otitis Media Clinical Trials

Furlow Palatoplasty With Tensor Tenopexy

Start date: February 28, 2012
Phase: N/A
Study type: Interventional

This study compares a standard method for palate repair (the Furlow palatoplasty) with a modification of that method to determine which, if either, is more effective in reducing the duration of middle-ear disease (fluid in the ear) in cleft palate patients.

NCT ID: NCT01500109 Completed - Cleft Palate Clinical Trials

Efficacy of Oral Versus Intravenous Acetaminophen for Primary Pediatric Cleft Palate Repair

Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of this investigator-initiated study is to determine whether acetaminophen is an effective pain reliever for primary cleft palate repair in children and possesses opioid sparing effects. Additionally, the investigators will determine if patients who receive acetaminophen have less opioid related side-effects. The study will have three study groups based on whether the patient receives Ofirmev® and opioids (Fentanyl and Morphine), oral acetaminophen elixir and opioids (Fentanyl and Morphine), or opioids (Fentanyl and Morphine) alone. Total opioid (Fentanyl and Morphine) consumption will be tracked for the intraoperative period and 24 hours after surgery for all patients within the study and converted to morphine equivalents.

NCT ID: NCT01380171 Completed - Cleft Palate Clinical Trials

Primary Palatoplasty in Pediatric Patients - A Retrospective Review of Surgical Outcomes

Start date: February 2007
Phase: N/A
Study type: Observational

Children who are born with cleft palate need surgery in order to correct the problem. The surgery is needed because the defect allows food to leak into the nose. It also causes the patient to be unable to speak correctly, producing a problematic nasal sound. Sometimes the first surgery does not completely correct the problem and a second surgery is needed. Looking at the records of patients who have had corrective surgeries done in the past would allow the surgeons to improve their success rate and reduce the need for secondary surgeries. It would also create greater patient safety and reduce cost for families.

NCT ID: NCT01252264 Completed - Cleft Palate Clinical Trials

FaceBase Biorepository

Start date: November 2010
Phase:
Study type: Observational

The purpose of this study is to find out if there are any genetic differences between people with and without disorders of the head, face, and eye. We will create a biorepository of samples from people with and without these types of birth defects. A biorepository is a collection or "bank" of human tissue materials (such as blood or saliva) for research purposes. These samples will then be available to investigators studying these disorders.