Skip to content

The effectiveness of skeletal and dental of palatal expansion

A clinical trial to comparison the effectiveness of skeletal and dental of palatal expansion after miniscrew-assisted fixed with conventional method in patients who need orthodontic treatment and palatal expansion

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017022632787N1
Enrollment
74
Registered
2017-03-01
Start date
2017-03-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Orthodontic treatment and palatal expansion. Other specified medical care

Interventions

Intervention 1: Control group: Who are revising conventional appliance Hyrax based on dental for palatal expansion, the effectiveness of skeletal and dental are examining 4 months after intervention.
Control group: Who are revising conventional appliance Hyrax based on dental for palatal expansion, the effectiveness of skeletal and dental are examining 4 months after intervention.
Intervention group: Who are revising miniscrew-assisted fixed for palatal expansion, the effectiveness of skeletal and dental are examining 4 months after intervention.

Sponsors

Vice Chancellor for Research, Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 16 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: who need to maxillary arches expand; aged between 12 and 16 years; who show pre-puberty stage (before CS3) based on cervical vertebral stadium (CVS). Exclusion criteria: In maturity or later of CS3 stages; having certain systemic diseases; using medications that impact on orthopedic and orthodontic response; who patients need to using other appliance (face mask, etc.) simultaneously with expansion appliance.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The effectiveness of skeletal and dental including rate of disruption hyoid, rate of tipping crown, gingival recession, fenestration/dehiscence. Timepoint: 4 months after intervention. Method of measurement: Cone beam computed tomography (CBCT).

Secondary

MeasureTime frame
Root recession. Timepoint: 4 months after intervention. Method of measurement: Appliance expansion.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzin Heravi

Mashhad Faculty of Dentistry

farzinheravi@gmail.com+98 51 3806 7224

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026