CompletedNot Applicable

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

Syria16 participantsStarted 2018-08-29

Plain-language 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.

Who can participate

Age range18 Years – 28 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Class I malocclusion with moderate crowding (4-6 mm of a tooth-size-arch-length-discrepancy).
✓. Good oral hygiene and periodontal health.
✓. No severe skeletal discrepancy.
✓. Normal proclination for the upper and lower incisors.
✓. No congenitally missing or extracted teeth (except for the third molars).

Exclusion criteria

✕. Bimaxillary dentoalveolar severe protrusion.
✕. Previous orthodontic treatment.
✕. Subject with psychological abnormalities.
✕. Subject with systemic diseases.

What they're measuring

Change in perception of pain

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks

Change in perception of discomfort

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks

Change in the feeling of swelling

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks

Change in the difficulty of mastication

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks

Change in difficulty swallowing

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks]

Change in the limits of opening the mouth

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks

Trial details

NCT IDNCT04728464

SponsorDamascus University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2020-07-01

View on ClinicalTrials.gov More Crowding of Anterior Mandibular Teeth trials

Plain-language summary

Who can participate

Age range18 Years – 28 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Class I malocclusion with moderate crowding (4-6 mm of a tooth-size-arch-length-discrepancy).
✓. Good oral hygiene and periodontal health.
✓. No severe skeletal discrepancy.
✓. Normal proclination for the upper and lower incisors.
✓. No congenitally missing or extracted teeth (except for the third molars).

Exclusion criteria

✕. Bimaxillary dentoalveolar severe protrusion.
✕. Previous orthodontic treatment.
✕. Subject with psychological abnormalities.
✕. Subject with systemic diseases.

What they're measuring

Change in perception of pain

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks

Change in perception of discomfort

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks

Change in the feeling of swelling

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks

Change in the difficulty of mastication

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks

Change in difficulty swallowing

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks]

Change in the limits of opening the mouth

Timeframe: (1) one day following the beginning of the treatment, (2) after a week of the beginning of treatment, (3) after 2 weeks, (4) after 4 weeks