Clinical Trials Directory

Trials / Completed

CompletedNCT04728464

Pain, Acceptance, and Discomfort With Periodontally Accelerated Osteogenic Orthodontics (PAOO)

Evaluation of the Levels of Pain and Discomfort of 'Periodontally Accelerated Osteogenic Orthodontics' (PAOO) in the Leveling and Alignment of Crowded Lower Anterior Teeth: A Prospective Non-controlled Cohort Study

Status
Completed
Phase
Study type
Observational
Enrollment
16 (actual)
Sponsor
Damascus University · Academic / Other
Sex
All
Age
18 Years – 28 Years
Healthy volunteers
Not accepted

Summary

Patients will be examined in the Orthodontic Department of the University of Damascus Dental School. Patients who will be treated in conjunction with the PAOO procedure and subjects who will meet the inclusion criteria will be included then the initial diagnostic records (diagnostic gypsum models, internal and external oral photographs, as well as radiographic images) will be studied to ensure that the selection criteria will be accurately matched. This study aims to assess patients' acceptance of the PAOO procedure as well as the levels of pain and discomfort associated with this treatment.

Detailed description

Surgical procedure associated with PAOO The surgery will be performed under local anesthesia and then full-thickness flaps will be reflected labially only from the distal surface of the lower right canine to the distal surface of the lower left canine, after washing the exposed alveolar bone with saline, then a selective cortical cutting will be performed using a piezosurgery and then the Bone-D® xenograft (particle size of 0.2 mm-1.0 mm) from Medpark (Busan, Korea) will be placed, then the wound will be sutured. Then a schedule will be set up to review the patient after 1, 7, 14, and 28 days to fill out questionnaires related to pain, acceptance, discomfort, satisfaction, and follow-up to orthodontic treatment.

Conditions

Interventions

TypeNameDescription
PROCEDUREPeriodontally Accelerated Osteogenic Orthodontics (PAOO)Fixed appliance will be placed for every patient, then surgical procedure will be applied after reflecting a full-thickness labial flap.

Timeline

Start date
2018-08-29
Primary completion
2020-07-01
Completion
2020-11-01
First posted
2021-01-28
Last updated
2021-02-02

Locations

1 site across 1 country: Syria

Source: ClinicalTrials.gov record NCT04728464. Inclusion in this directory is not an endorsement.