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Clinical Trial

Clinical Performance of Direct-Printed Versus Thermoformed Aligners

NCT: NCT07637227 · RECRUITING

NCT IDNCT07637227
StatusRECRUITING
Start Date2026-06
Completion2027-10
SponsorUniversity of Baghdad (OTHER)
First posted
Last updated

Brief Summary

The goal of this study is to evaluate and compare the clinical effectiveness of in-office directly 3D-printed clear aligners versus conventional multilayered thermoformed aligners. The main question it aims to answer is: Does the use of in-office direct-printed shape-memory aligners result in superior clinical effectiveness, compared to established multilayer thermoformed aligner systems? Researchers will compare a Direct-Printed Aligner (DPA) group using Senertek Clear-A V2 resin to a Thermoformed Aligner (TFA) group using Zendura FLX multilayer sheets to see if the additive manufacturing process improves clinical outcomes and patient satisfaction. Participants will: * Undergo initial records including intraoral digital scans, photos, and a panoramic radiograph for treatment planning. * Wear their assigned clear aligners (either direct-printed or thermoformed) for at least 22 hours per day, changing them every 7 days. * Attend follow-up appointments every 5 weeks.

Frequently Asked Questions

What is Clinical Performance of Direct-Printed Versus Thermoformed Aligners?

Clinical Performance of Direct-Printed Versus Thermoformed Aligners is a clinical trial registered under NCT07637227. Current status: RECRUITING.

What is the status of NCT07637227?

The current status of NCT07637227 (Clinical Performance of Direct-Printed Versus Thermoformed Aligners) is: RECRUITING.

When did Clinical Performance of Direct-Printed Versus Thermoformed Aligners start?

Clinical Performance of Direct-Printed Versus Thermoformed Aligners started on 2026-06.

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Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.