Accuracy of Maxillary Repositioning With bi or Tripartite Disjonction by

See also
Status	Clinical Trial	Phase
Completed	`NCT03621891` - Alterations in Subgingival Microbiota and Hypoxia in Occlusal Trauma
Completed	`NCT05960500` - All on Six Versus Parallel Implant Distribution for Maxillary Denture Opposing Mandibular All on Four	N/A
Completed	`NCT03804034` - Importance of Neurogenic Inflammation in the Angiogenic Response of the Dental Pulp as a Defensive Response	N/A
Completed	`NCT06159530` - Effect Of Occlusal Materials Used For All On Four Mandibular Implant Prosthesis With PEEK Framework	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT03621891 - Alterations in Subgingival Microbiota and Hypoxia in Occlusal Trauma

Completed

NCT05960500 - All on Six Versus Parallel Implant Distribution for Maxillary Denture Opposing Mandibular All on Four

N/A

Completed

NCT03804034 - Importance of Neurogenic Inflammation in the Angiogenic Response of the Dental Pulp as a Defensive Response

N/A

Completed

NCT06159530 - Effect Of Occlusal Materials Used For All On Four Mandibular Implant Prosthesis With PEEK Framework

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT05186376
Study type	Observational
Source	Centre Hospitalier Universitaire de Nice
Contact
Status	Completed
Phase
Start date	May 1, 2021
Completion date	July 21, 2021

Accuracy of Maxillary Repositioning With bi or Tripartite Disjonction by Virtual Planning in Orthognathic Surgery Using Patient-specific Titanium Plates

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms