Clinical Trials Logo

Cleft Palate clinical trials

View clinical trials related to Cleft Palate.

Filter by:

NCT ID: NCT03877666 Recruiting - Clinical trials for Cleft Lip and Palate

Assessment of the Influence of Cleft Repair on Microcirculation of the Palate

Start date: August 4, 2020
Phase:
Study type: Observational

Investigators aim to evaluate the influence of cleft surgery on the tissue microcirculation of the palate with a non-invasive measurement.

NCT ID: NCT03868891 Terminated - Cleft Palate Clinical Trials

Exercises for Improving Soft Palate and Eustachian Tube Function in Children With Ear Tubes With or Without Cleft Palate

Start date: August 16, 2019
Phase: N/A
Study type: Interventional

Elevation of the soft palate (the soft part of the roof of the mouth) during swallowing helps the Eustachian tube to open and keep the ear healthy. (The Eustachian tube is the normal tube running from the middle ear to the back of the nose and throat). When the soft palate does not move enough (due to a history of cleft palate or for unknown reasons), this can lead to speech problems. Also, because the Eustachian tube is not opening enough, fluid can accumulate in the middle ear, which requires treatment with ear tubes. The goal of this research study is to determine if soft palate exercises will help improve the ability of the soft palate to close the area between the throat and nose, like it is supposed to during speech and swallowing, and if this improves Eustachian tube opening.

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: NCT03837652 Not yet recruiting - Cleft Palate Clinical Trials

Bone-borne Palatal Expander With Corticotomy for Cleft Palate Patients

Start date: February 2019
Phase: N/A
Study type: Interventional

The tooth-borne palatal expander has limitations in the subset of patients with scarred, constricted cleft palate. At times, although posterior expansion is successful, transverse expansion of the anterior palate (near the alveolar cleft) is inadequate. Will the application of bone borne palatal expander combined with a corticotomy be more effective in the expansion of the constricted maxilla in cleft palate patients?

NCT ID: NCT03799068 Active, not recruiting - Block Clinical Trials

Suprazygomatic Nerve Block vs Surgical Site Infiltration in Cleft Palate Repair

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the efficacy and duration of effect of bupivacaine given preoperatively as a bilateral suprazygomatic maxillary nerve block and to compare it with peri-incisional infiltration with the same agent for perioperative analgesia in children undergoing cleft palate repair.

NCT ID: NCT03720990 Completed - Clinical trials for Smith-Lemli-Opitz Syndrome

Smith-Lemli-Opitz Syndrome and Cholic Acid

Start date: March 27, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether dietary cholic acid therapy benefits people with Smith-Lemli-Opitz syndrome (SLOS) by leading to an increase in plasma cholesterol and reduction in harmful cholesterol precursors. SLOS participants will be treated with dietary cholic acid for 8 weeks and plasma cholesterol and cholesterol precursor metabolites will be measured.

NCT ID: NCT03688737 Not yet recruiting - Laser Clinical Trials

Low Level Laser in Isolated Cleft Palate Repair Versus Surgical Correction Without LLL in Healing Process

Start date: October 2018
Phase: N/A
Study type: Interventional

Does the use of low level laser (LLL) after surgical correction of cleft palate improve healing and decrease incidence of oronasal fistula?

NCT ID: NCT03632044 Enrolling by invitation - Cleft Palate Clinical Trials

Evaluation of Trigeminal Nerve Blockade

Start date: November 20, 2018
Phase: Phase 4
Study type: Interventional

Cleft palate repair requires high doses of opioids for pain control postop. An alternative approach is placement of nerve blocks in the pterygopalatine fossa bilaterally, blocking the maxillary nerve & covering the entire midface. Application of bilateral suprazygomatic maxillary nerve blockade of the infraorbital nerve may provide effective analgesia for cleft lip repair, improving time to oral intake, pain control and time to hospital discharge.

NCT ID: NCT03585608 Completed - Cleft Palate Clinical Trials

Optic Nerve Sheath Diameter in Patients Undergoing Palatoplasty

Start date: July 18, 2018
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to evaluate the change of the optic nerve sheath diameter according to the change of the neck position in pediatric patients undergoing palatoplasty.

NCT ID: NCT03572907 Withdrawn - Cleft Palate Clinical Trials

Use of Titanium Plate in Rhinoplasty in Patients With Cleft Lip and Palate : Aesthetic and Functional Impact.

PETROL/TROPHIC
Start date: October 2018
Phase:
Study type: Observational

The patients in this study are all born with a cleft lip and palate. They underwent several interventions in childhood to take care of it. Professor Gleizal offered them a secondary rhinoplasty aimed at normalizing the appearance of their nose. In this malformative and multioperated context, typical nasal deformities affect the tip of the nose, which appears to be sagging and asymmetrical. Scarred soft tissues exert an important retractile force against which conventional rhinoplasty techniques often remain insufficient. The use of columellar struts makes it possible to give again projection to the tip of the nose but when this strut is made from cartilage or bone, it is absorbed with the time. Moreover, these interventions require a remote removal of the site of interest (costal cartilage, tibial crest, calvaria) which generates additional morbidity. The investigators propose an alternative using a synthetic graft of titanium. This material has been used for many years for its excellent biocompatibility and trauma resistance. 28 patients were able to benefit from this technique between March 1, 2016 and March 1, 2018. The investigators wish to evaluate the aesthetic and functional results from the patient's point of view by submitting them to one validated rhinoplasty questionnaire after the end of the patient's inclusion.