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Piezocision with & without osteoperforation

Comparison of two surgical methods, Piezocision with & without osteoperforation in maxillary canine retraction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200826048536N1
Enrollment
15
Registered
2020-10-20
Start date
2020-10-16
Completion date
Unknown
Last updated
2020-11-09

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

Conditions

Patients who need maxillary first premolar extraction.

Interventions

Intervention 1: First intervention group: Piezocision surgery with Acteon piezotome, with creating three areas of osteoperforation (microcorticotomy) using No.3 surgery tip via soft tissue tunneling.

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 25 Years

Inclusion criteria

Inclusion criteria: Patients need to first premolar extraction Patients need to canine retraction

Exclusion criteria

Exclusion criteria: Patients with history of previous orthodontic therapy Patients having systemic disease Patients with history of using chemotherapy drugs and bisphosphonates

Design outcomes

Primary

MeasureTime frame
Maxillary canine retraction. Timepoint: One week after surgery and three months after surgery. Method of measurement: Sirona sacnner and autocad software.

Secondary

MeasureTime frame
Maxillary first molar movement. Timepoint: One week after surgery and three months after surgery. Method of measurement: Sirona scanner and autocad software.;Maxillary canine rotation. Timepoint: One week after surgery and three months after surgery. Method of measurement: Sirona scanner and autocad software.;Maxillary canine inclination. Timepoint: One week after surgery and three months after surgery. Method of measurement: Sirona scanner and autocad software.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAnita Babadi

Ahvaz University of Medical Sciences

babadi.a@ajums.ac.ir+98 61 3223 4716

Outcome results

None listed

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