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Effects of Invisalign Palatal Expander System

Not Applicable
Recruiting
Conditions
Palatal Expansion Technique
Registration Number
NCT06414863
Lead Sponsor
University of the Pacific
Brief Summary

The aim of this study is to evaluate the effectiveness of Invisalign Palatal Expander system ingrowing patients. This study compares the treatment outcomes of Invisalign Palatal Expander system to conventional treatments through randomized controlled trial.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
120
Inclusion Criteria

Not provided

Exclusion Criteria
  1. Any general medical health problems which may influence treatment
  2. Any craniofacial anomalies
  3. Skeletal Class III patients
  4. Mixed dentition patients with more than 2 heavily restored primary second or permanent first molars.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Arch width change12-18 months

Arch width change measured on digital study casts

Width change12-18 months

Transverse changes on CBCTs

Secondary Outcome Measures
NameTimeMethod
Cephalometric changes12-18 months

Common Cephalometric measurements changes on CBCT analysis

Trial Locations

Locations (1)

University of the Pacific

🇺🇸

San Francisco, California, United States

University of the Pacific
🇺🇸San Francisco, California, United States
Heeyeon Suh
Contact
415-351-7134
hsuh1@pacific.edu

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