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NCT05684601

Impact of 3D Intraoral Scanning on Postsurgical Evaluation of Mandibular Third Molar Surgery

Completed NA Last updated 13 January 2023
What this trial tests

NA trial testing Third molar surgery in Third Molar Surgery in 56 participants. Completed in 20 October 2022.

Timeline
15 September 2020
Primary endpoint
20 October 2022
20 October 2022

Quick facts

Lead sponsorUniversity of Catania
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment56
Start date15 September 2020
Primary completion20 October 2022
Estimated completion20 October 2022
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

University of Catania

Who can join

Adults 18 to 65, any sex, with Third Molar Surgery or Impacted Third Molar Tooth. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study was to analyze the effectiveness of piezoelectric surgery and traditional rotating device in reducing perioperative sequelae after impacted mandibular third molar surgery in 56 subjects. Ni All subjects were randomly allocated to receive one treatment.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Third molar surgery

Trials testing the same drug.

Other recruiting trials for Third Molar Surgery

Currently open trials in the same condition.

Other University of Catania trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05684601.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing