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Cleft Palate clinical trials

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NCT ID: NCT02688634 Withdrawn - Cleft Palate Clinical Trials

The Role of Antibiotic Prophylaxis in Cleft Palate and Velopharyngeal Insufficiency Repair

Cleft Palate
Start date: April 2016
Phase: N/A
Study type: Observational

Cleft Lip and Palate surgical repair is one of the most common procedures performed by Plastic and Reconstructive Surgeons in the World. With this in mind, it is curious that no consensus exists regarding the usage of postoperative antibiotics or the effects this might have on wound complications such as cellulitis, dehiscence, or fistula formation. The surgical bed in cleft lip/palate repair is known to harbor a myriad of pathological organisms, indeed the human bite is one of the more clinically and microbiologically significant injuries to treat. This research study is to elucidate the role, if any, that prophylactic antibiotics have in the prevention of complications post cleft palate (CP) and VPI repair and potentially establish a new paradigm of care.

NCT ID: NCT02658318 Completed - Cleft Palate Clinical Trials

Postoperative Complications After Cleft Palate Closure in Patients With Pierre Robin Sequence: Operative Considerations

Start date: January 2011
Phase: N/A
Study type: Observational

In cleft surgery there is no current general agreement on the treatment strategy of patients with the Pierre Robin Sequence. The timing of surgery and the surgical approach depends on the treating physician or the hospital facility. Literature regarding peri- and postoperative complications in the target population are lacking. The investigators aim to retrospectively review the charts of all cleft patients, both PRS and non-PRS, treated with an adapted Furlow palatoplasty between 01/01/2011 and 31/08/2015. The incidence of peri- and postoperative complications, with a specific focus on respiratory complications, will be examined. The value of demographic, surgical and postoperative parameters will be examined as potential risk factors for the development of complications.

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: NCT02583100 Completed - Cleft Palate Clinical Trials

Improving Outcomes in Cleft Palate Surgery

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

This is a pilot study to determine if an audit and feedback intervention decreases complication rates after cleft palate surgery.

NCT ID: NCT02422056 Completed - Hemorrhage Clinical Trials

Acid Tranexamic Effectiveness in Reducing the Intraoperative Bleeding in Palatoplasty

Start date: December 2013
Phase: Phase 4
Study type: Interventional

Randomized study evaluating the role of tranexamic acid in reducing intraoperative bleeding in palatoplasty.

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: 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.