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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT02221206
Date of registration: 18/08/2014
Prospective Registration: No
Primary sponsor: Zhejiang University
Public title: Volumetric Analysis of Root Resorption With Mini-Screw Implant Anchorage-assisted Retraction of Maxillary Incisors
Scientific title: Clinical Observation for the Root Resorption With Mini-Screw Implant Anchorage-assisted Retraction of Maxillary Incisors
Date of first enrolment: August 2014
Target sample size: 60
Recruitment status: Active, not recruiting
URL:  http://clinicaltrials.gov/show/NCT02221206
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment  
Phase:  N/A
Countries of recruitment
China
Contacts
Name:     Mengjie Wu, MD, DDS
Address: 
Telephone:
Email:
Affiliation:  Department of Orthodontics, Hospital of Stomatology, Zhejiang University
Key inclusion & exclusion criteria

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



Age minimum: 18 Years
Age maximum: 25 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Dental Dysgnathia
Intervention(s)
Device: Mini-Screw implant
Primary Outcome(s)
Root resorption [Time Frame: 10 months after implant insertion]
Secondary Outcome(s)
Secondary ID(s)
NSF81371167
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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