Efficacy of Injectable Platelet Rich Fibrin (i-PRF) in Enhancing Bone Quality (NCT03399760) | Clinical Trial Compass
CompletedNot Applicable
Efficacy of Injectable Platelet Rich Fibrin (i-PRF) in Enhancing Bone Quality
Syria20 participantsStarted 2017-08-20
Plain-language summary
Twenty patients need therapeutic extraction of the maxillary first premolars with subsequent retraction of the maxillary canines, will be divided randomly into two groups, and will randomly assigned to one side of the maxillary arch at the first premolar region, and the other side served as the control. Canine retraction will be initiated after completion of the leveling and alignment phase via closed nickel-titanium coil springs applying 150 g of force per side. Soldered transpalatal arch will be used as an anchor unit. The dento-alveolar changes will be assessed immediately before retraction and after 6 months using CBCT.
Who can participate
Age range15 Years – 27 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Adult healthy patients, Male and female, Age range: 15-27 years.
✓. Class II Division 1 malocclusion:
✓. permanent occlusion.
✓. Exist all the upper teeth (except third molars).
✓. Good oral and periodontal health:
Exclusion criteria
✕. Medical problems that affect tooth movement (corticosteroid, NSAIDs, …)
✕. patients have anti indication for oral surgery ( medical - social - psycho)
✕. Presence of primary teeth in the maxillary arch
✕. Missing permanent maxillary teeth (except third molars).
✕. Poor oral hygiene or Current periodontal disease:
✕. Patient had previous orthodontic treatment
What they're measuring
1
Canine root resorption
Timeframe: After 6 months from the beginning of canine retraction