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Volumetric Analysis of Root Resorption With Mini-Screw Implant Anchorage-assisted Retraction of Maxillary Incisors

Zhejiang University logo

Zhejiang University

Status

Unknown

Conditions

Dental Dysgnathia

Treatments

Device: Mini-Screw implant

Study type

Interventional

Funder types

Other

Identifiers

NCT02221206
NSF81371167

Details and patient eligibility

About

The intended study is designed as a prospective randomized controlled trial (RCT), comparing and contrasting the effect of mini-screw implant anchorage-assisted versus regular maximum anchorage by retracting the maxillary incisors.

Full description

The objective of the clinical study proposal will be to investigate the performance of early root resorption in order to find out if the magnitude and direction of retraction is appropriate for the retraction of maxillary incisors following the mini-screw anchorage.

Therefore, the study will compare and contrast the efficacy and results of the volumetric measurement by CBCT.

Patients

Males or females whose diagnoses require implant anchorage treatment will be included in the study. Inclusion criteria for the study are as followings:

Orthodontic indication for skeletal anchorage Adequate bone quantity for a palatal implant in the CBCT Good oral hygiene and normal wound healing capacity

Enrollment

60 estimated patients

Sex

All

Ages

18 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Orthodontic indication for skeletal anchorage
  • Adequate bone quantity for a palatal implant in the CBCT
  • Good oral hygiene and normal wound healing capacity

Exclusion criteria

  • Patients with cheilognathopalatoschisis and other system syndromes associated with craniofacial anomalies
  • Patients with immunodeficiency, diseases requiring a prolonged steroid usage, previous radiation therapy or chemotherapy
  • Patients with metabolic bone diseases or uncontrolled endocrine disorders
  • Alcohol or drug abuse
  • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Treatment
Active Comparator group
Description:
mini-screw implant anchorage-assisted retraction of maxillary incisors
Treatment:
Device: Mini-Screw implant
Control
No Intervention group
Description:
regular maximum anchorage

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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