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Using Platelet Rich Plasma in Reducing Alveolar Bone Resorption During Rapid Maxillary Expansion - Trial NCT03028038

Access comprehensive clinical trial information for NCT03028038 through Pure Global AI's free database. This Phase 1 trial is sponsored by Damascus University and is currently Completed. The study focuses on Bone Resorption. Target enrollment is 16 participants.

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NCT03028038
Phase 1
Completed
drug
Trial Details
ClinicalTrials.gov โ€ข NCT03028038
View on ClinicalTrials.gov
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Using Platelet Rich Plasma in Reducing Alveolar Bone Resorption During Rapid Maxillary Expansion
Evaluation of Efficacy of Injectable Platelet-Rich Plasma (PRP) in Reducing Alveolar Bone Resorption Following Rapid Maxillary Expansion (RME): A Cone Beam Computed Tomography (CBCT) Assessment

Study Focus

Bone Resorption

Platelet Rich Plasma

Interventional

drug

Sponsor & Location

Damascus University

Damascus, Syrian

Timeline & Enrollment

Phase 1

Jul 01, 2016

Jul 15, 2018

16 participants

Primary Outcome

Changes in buccal alveolar bone height loss and thickness reduction amount

Summary

The purpose of this study is to determine if the injection of Platelet-rich plasma (PRP) is
 effective in reducing alveolar bone loss that happens after each rapid maxillary expansion
 (RME) on the buccal aspect of the posterior teeth.
 
 16 patients with a skeletal maxillary constriction aged between 10-16 years old will get into
 orthodontic treatment to widen the maxilla using Hyrax appliance.
 
 An amount of patient blood will be withdrawn and centrifuged to get PRP. Then the PRP will be
 injected in one half of each patient mouth in a split-mouth design, beneath the buccal
 periosteal of the first molars and first premolars, the halves will be chosen randomly.
 
 High resolution CBCT images will be taken before and after orthodontic treatment to analyze
 buccal bone thickness and height changes.

ICD-10 Classifications

Osteolysis
Pathological resorption of teeth
Bone donor
Postsurgical malabsorption osteoporosis
Postsurgical malabsorption osteoporosis with pathological fracture

Data Source

ClinicalTrials.gov

NCT03028038

Non-Device Trial