Clinical trial

Assessment of Different Orthodontic Tooth Movements Assisted With Low-level Laser Therapy vs. Injectable Plasma-rich Fibrin: A Comparative Clinical Investigation

Name
923/91
Description
The present prospective clinical study will be undertaken for assessment of the effect of application of Injectable plasma-rich fibrin versus Low-Level Laser Therapy onthe rate of different orthodontic tooth movements,
Trial arms
Trial start
2023-08-01
Estimated PCD
2024-02-01
Trial end
2024-09-01
Phase
Early phase I
Treatment
Low-level Laser Therapy vs. Injectable Platelets-rich Fibrin
laser and platelet rich fibrin
Arms:
I-PRF group: Intrusion, I-PRF groupMolar distalization group inrervention side, LLLT group: Intrusion, LLLT group: distalization intervntion side, LLLT group: leveling and alignment, LLLT side canine retraction, i-PRF group: leveling and alignment, i-PRF side: canine retraction
Size
82
Primary endpoint
assessment of the effect of application of Injectable plasma-rich fibrin versus Low-Level Laser Therapy on the accelration rate of different orthodontic tooth movements by millimeter
6 months
Eligibility criteria
Inclusion Criteria: A- leveling and alignment Eligibility criteria 1. Complete permanent dentition (third molars not included). 2. Moderate mandibular anterior crowding (with Little's irregularity index score greater than 4 mm) who required nonextraction approach in the mandibular arch. 3. No tooth size, shape or root abnormalities visible on patient's radiographic records. 4. No spaces in the mandibular arch. 5. No blocked out tooth that did not allow for placement of the bracket at the initial bonding appointment. 6. No required management with interproximal stripping, intermaxillary elastics, open NiTi springs, and removable or extra-oral devices. Maxillary molar distalization Inclusion criteria: 1. Age ranges from 14 to 17 years. 2. Bilateral Class II molar relationship. 3. Skeletal Class I or mild Class II relationship. 4. Normal or decreased vertical height. 5. No posterior crowding or spaces. 6. Fully erupted maxillary first and second molars. 7. Congenitally missing or extracted third molars. 8. Good oral hygiene. 9. Absence of any periodontal disease and alveolar bone loss. 10. Absence of medications that may inhibit orthodontic movement * Lower incisor leveling and alignment Inclusion criteria 1. Complete permanent dentition (third molars not included); 2. Moderate mandibular anterior crowding (with little's irregularity index score greater than 4 mm) who required non-extraction approach in the mandibular arch; 3. No tooth size, shape or root abnormalities visible on the patient's radiographic records; 4. No spaces in the mandibular arch; 5. No blocked out tooth that did not allow for placement of the bracket at the initial bonding appointment; 6. No required management with interproximal stripping, inter-maxillary elastics, open NiTi springs, and removable or extra-oral devices. Canine retraction Eligibility criteria 1. Age, 15 to 25 years; 2. Class ii division 1 malocclusion with mild or no crowding; 3. No previous orthodontic treatment; 4. No systemic disease that might have affected bone formation or density, such as osteoporosis, hyperparathyroidism, or vitamin d deficiency; 5. Adequate oral hygiene; 6. Probing depth values not exceeding 3 mm across the 7. Entire dentition; 8. Adequate thickness of the attached gingiva (1-2 mm); 9. No radiographic evidence of bone loss Exclusion Criteria:Exclusion criteria: 1. Patients who required surgery to correct skeletal discrepancies. 2. Patients with congenital dentoskeletal disorders. 3. Missed or mutilated teeth in maxillary arch. 4. Patients with poor oral hygiene and/or periodontally compromised patients Severe dental crowding that necessitates an extraction approach 2. Abnormal anteroposterior and vertical relationships; 3. Patients with cleft lip and palate, anomalies, and syndromes; 4. Previous orthodontic 5. Treatment; 6. Regular medications intake that could interfere with otm. -
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'FACTORIAL', 'interventionModelDescription': 'Factorial Assignment', 'primaryPurpose': 'BASIC_SCIENCE', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 82, 'type': 'ESTIMATED'}}
Updated at
2023-08-01

1 organization

1 product

1 indication