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Dental Occlusion, Traumatic clinical trials

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NCT ID: NCT03887975 Completed - Clinical trials for Edentulous Alveolar Ridge

T-Scan Study of Occlusion in Case of Implant Retained Overdenture

Start date: February 20, 2018
Phase: N/A
Study type: Interventional

Materials and methods: fourteen patients were selected according to the inclusion criteria, the participants were stratified equally into two groups, patients were assigned to receive either monoplane or lingualized occlusal schemes to their overdentures. For each patient placement of two mini-implants in the mandible at the canine region was done, bar joint attachment was used to splint the mini implants. Each implant was 2.5 mm in diameter and 10 mm in length. T-scan occlusal load analysis records were done in centric occlusion , the records was used to analyze the biting force of the denture as a Full Closure Force Movie recording, then Time vs. Force Graph of that Force Movie is accomplished. T-scan records were taken three times for each patient in the two groups ,Immediately after loading ,three months and six months of loading.

NCT ID: NCT03648125 Terminated - Clinical trials for Dental Occlusion, Traumatic

Influence of Dental Occlusion on the Performance of High Level Rowers (IODPR)

IODPR
Start date: October 27, 2017
Phase: N/A
Study type: Interventional

Monocentric, prospective, randomized, open-label, cross-over study.

NCT ID: NCT02678715 Terminated - Clinical trials for Temporomandibular Joint Dysfunction Syndrome

Effectiveness of Three Oral Devices as Mouthguard in Electroconvulsive Therapy. Randomized Crossover Clinical Trial.

Start date: February 2016
Phase: N/A
Study type: Interventional

This observer-blind crossover intervention study aims to determine the most effective type of device as oral mouthguard in modified-Electroconvulsive Therapy (m-ECT) comparing three types of devices: standard, prefabricated and manufactured in the dental laboratory. Patients from the ECT Unit of Psychiatric Department of the University Hospital of Bellvitge will use the three devices at a random sequence during the twelve treatment sessions, so each device (A, B, C) will be used for two weeks, that is, for four consecutive sessions.

NCT ID: NCT00328224 Completed - Dental Caries Clinical Trials

Oral Status and Prevalence of Dental Trauma in Children Treated With Ritalin Due to Attention-Deficit Hyperactivity Disorder (ADHD)

Start date: May 2006
Phase: N/A
Study type: Observational

To evaluate the dental status of children using ritalin and suffering from ADHA in comparison to healthy children.