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NCT04670211: SARPE

Observational Comparison of Tooth-borne, Bone-borne and Hybrid Distraction Following SARPE.

Status unknown Last updated 20 April 2021
What this trial tests

trial testing maxillary distractor in Malocclusion in 90 participants. Status unknown.

Timeline
1 May 2021
Primary endpoint
31 December 2023
31 December 2023

Quick facts

Lead sponsorZOL
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment90
Start date1 May 2021
Primary completion31 December 2023
Estimated completion31 December 2023

Drugs / interventions tested

Conditions studied

Sponsor

ZOL — full company profile →

Who can join

12 and older, any sex, with Malocclusion. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The investigators will perform a prospective, non-randomized observational study. The aim of this study is to evaluate stability of tooth-borne, bone-borne and hybrid expansion following SARPE by using data collected according to the existing SARPE follow-up protocol. The insights of this study might elucidate the preferred expansion technique and improve surgical technique.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Malocclusion

Currently open trials in the same condition.

Other ZOL 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/NCT04670211.

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