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Palatal Expansion Technique

Tundra lists 5 Palatal Expansion Technique clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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NOT YET RECRUITING

NCT07734688

Miniscrew-Assisted Rapid Palatal Expansion for Obstructive Sleep Apnea

The goal of this clinical trial is to learn whether miniscrew-assisted rapid palatal expansion (MARPE) can improve obstructive sleep apnea (OSA) in late adolescents and adults aged 16 to 60 years. The main questions it aims to answer are: 1. Does MARPE improve sleep apnea severity, as measured by Home Sleep Apnea Testing (HSAT), including respiratory event index (REI), oxygen desaturation index (ODI), mean oxygen saturation, nadir oxygen saturation, snoring events, and body position? 2. Does MARPE improve breathing and sleep-related symptoms, including upper airway dimensions, daytime sleepiness, quality of life, and peak nasal inspiratory flow (PNIF)? Researchers will compare a MARPE group with a control group that receives standard care for obstructive sleep apnea for 3 months to see whether MARPE provides additional benefit. Participants will: 1. Receive standard care for obstructive sleep apnea 2. Be randomly assigned to either MARPE plus standard care or standard care alone for 3 months 3. In the MARPE group, wear a miniscrew-assisted rapid palatal expander and activate it according to the study protocol 4. Visit the clinic for follow-up care and monitoring 5. Data will be collected at baseline (T0) and 3 months (T1). At both time points, participants in the MARPE group will be assessed using Home Sleep Apnea Testing (HSAT), cone beam computed tomography (CBCT), Epworth Sleepiness Scale (ESS), Functional Outcomes of Sleep Questionnaire Short Version (FOSQ-10), and peak nasal inspiratory flow (PNIF). Participants in the control group will be assessed using HSAT, ESS, FOSQ-10, and PNIF.

Gender: All

Ages: 16 Years - 60 Years

Updated: 2026-07-29

OSA - Obstructive Sleep Apnea
Palatal Expansion Technique
NOT YET RECRUITING

NCT07611227

Teleorthodontics Versus Conventional Follow-up During Early Interceptive Orthodontic Treatment in Children

The goal of this clinical trial is to learn if teleorthodontic remote monitoring is as effective as traditional in-office care for children undergoing Phase I expansion therapy. It will also evaluate whether this technology can safely reduce the frequency of unscheduled emergency appointments. Main Questions The study aims to answer the following: 1. Is remote monitoring non-inferior to conventional care in improving dental alignment, as measured by the Peer Assessment Rating (PAR) Index? 2. Does the use of weekly smartphone-based photo check-ins significantly lower the number of unscheduled emergency visits? 3. How does remote monitoring impact appliance compliance, parental satisfaction, and the child's level of distress during treatment? Comparison Researchers will compare a teleorthodontics group-which uses weekly smartphone photography and clinic visits every 8 weeks-to a conventional group receiving standard in-person follow-ups every 4 weeks. Participant Activities Participants will: 1. Commence Phase I treatment using a maxillary or mandibular expansion appliance. 2. If assigned to the teleorthodontics group, capture a standardized set of five intraoral photographs weekly via a dedicated smartphone application. 3. Attend scheduled in-office checkups every 4 or 8 weeks, depending on their assigned group. 4. Maintain a daily diary to record appliance activations and report on their treatment experience.

Gender: All

Ages: 7 Years - 11 Years

Updated: 2026-05-28

1 state

Teledentistry
Orthodontics, Interceptive
Palatal Expansion Technique
RECRUITING

NCT06246656

Evaluation of Hard and Soft Tissue Change During Maxillary Expansion Using a Computer-aided Design / Computer-aided Manufacturing Appliance.

* Hard tissue changes during the transversal expansion of the maxilla using a CAD/CAM expansion appliance. * Soft tissue changes during the transversal expansion of the maxilla using a CAD/CAM expansion appliance. Participants will undergo orthodontic treatment, including: * Initial records (intraoral scan, CBCT (cone-beam computed tomography) scan, face scan) * Placement of guided orthodontic TADs (Temporary Anchorage Devices) * Skeletal expansion using CAD/CAM appliance * Fixed multibracket appliance in the upper and lower jaw * Intermediate and terminal documents (intraoral scan, CBCT scan, face scan)

Gender: All

Ages: 12 Years - 26 Years

Updated: 2025-09-05

1 state

Palatal Expansion Technique
RECRUITING

NCT06267989

The Effectiveness of Early Intervention to Correct the Position of PDC:s

Approximately 2-3% of children will have problems with one or both of their permanent or 'adult' canine teeth in the upper jaw. These canine teeth sometimes fail to erupt properly, because they are displaced into the roof of the mouth or palate. These are known as palatally displaced canines, PDC, (Brin et al., 1986, Ericson and Kurol, 1987). In addition to failing to erupt, displaced teeth can cause problems, such as damage to the roots or displacement of the neighbouring teeth (Ericson and Kurol, 1988a, Ericson and Kurol, 2000, Falahat et al., 2008). It has been suggested that if the primary ('baby' or 'milk') canine is extracted at an appropriate time in a child with a suspected palatally displaced canine, then the displaced tooth might spontaneously correct its position (Ericson and Kurol, 1988b) and the extraction of the baby canine when a clinician suspects that the adult canine is displaced has become accepted clinical practice (Short, 2009). This appears to be on the basis of one report of a series of 35 children who received the intervention and no control group (Ericson and Kurol, 1988b). Two recent systematic reviews have examined the evidence for the effectiveness of removal of the primary canine with the aim of correcting the eruption path of a palatally displaced canine. A recent systematic review published in The Cochrane Library in 2021 (Benson et al., 2021) noted that the evidence for any intervention to correct the eruption path of a displaced permanent canine is weak and further research is required. Numerous problems with the reported studies were identified by both reviews. Other authors have suggested that using a RME (Rapid Maxillary expansion) or headgrear (EOT) to create sufficient space within the dental arch for the permanent canine tooth will encourage the tooth to erupt (Baccetti et al., 2011). This approach might be less traumatic to a child who may have had no experience of dental treatment, other than routine check-ups. If either or both approaches are shown to be effective then their widespread use would be advantageous to both the child and the healthcare provider, because the need for an operation, under general anaesthetic, to uncover the tooth and extensive brace treatment to straighten the tooth will be avoided.

Gender: All

Ages: 10 Years - 12 Years

Updated: 2025-04-24

Ectopic Tooth Eruption
Palatal Expansion Technique
Randomized Clinical Trial
RECRUITING

NCT06414863

Effects of Invisalign Palatal Expander System

The aim of this study is to evaluate the effectiveness of Invisalign Palatal Expander system ingrowing patients. This study compares the treatment outcomes of Invisalign Palatal Expander system to conventional treatments through randomized controlled trial.

Gender: All

Ages: 6 Years - 14 Years

Updated: 2024-05-16

1 state

Palatal Expansion Technique