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Clinical Trials/NCT05866965
NCT05866965
Completed
N/A

Effect of Platelet-rich Fibrin on Soft Tissue, Periodontal Pocket Healing and Alveolar Bone Height After Third Molar Surgery

Lam Cu Phong1 site in 1 country26 target enrollmentDecember 1, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Platelet-rich Fibrin
Sponsor
Lam Cu Phong
Enrollment
26
Locations
1
Primary Endpoint
distal bone resorption
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

A Randomized, controlled clinical trial and split-mouth design was performed to assess and compare the effect of platelet-rich fibrin (PRF) on soft tissue healing, periodontal pocket depth and alveolar bone height distal to second molar of the study and control groups after third molar surgical removal.

Sample include of participants who had indication of impacted lower third molars extraction on both sides with symmetrically orientation and same difficult index. All participants had same extraction protocol on both side at Department of Oral surgery, Faculty of Odonto-stomatology, University of Medicine and Pharmacy, Ho Chi Minh City.

Soft tissue healing, periodontal pocket depth and distal bone height were evaluation by an independent investigator.

Registry
clinicaltrials.gov
Start Date
December 1, 2019
End Date
December 1, 2021
Last Updated
2 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Lam Cu Phong
Responsible Party
Sponsor Investigator
Principal Investigator

Lam Cu Phong

Lecturer

University of Medicine and Pharmacy at Ho Chi Minh City

Eligibility Criteria

Inclusion Criteria

  • Patient over 18 years old.
  • Good general health.
  • Bilateral lower third molars equivalent in inclination and Pell and Gregory's impaction classification (classification II, III and B, C). The assessment of equivalence between two mandibular third molars was determined on the panoramic radiograph.
  • The difference of third molar inclination on both sides not greater than 15 degrees.
  • The patient consented to participate in the study after hearing clearly the explanation of purposes and requirements of the study.

Exclusion Criteria

  • Patients with any systemic disease contraindicated for surgery.
  • Presence of acute inflammation or infection at third molar areas.
  • Patients refused to participate in the study, did not comply with treatment or did not come to the follow-up examination as required.
  • The difference in surgical time between the two groups was more than 10 minutes.

Outcomes

Primary Outcomes

distal bone resorption

Time Frame: 6th postoperative month

resorption of alveolar bone height distal to second molar

periodontal pocket depth

Time Frame: 6rst postoperative month

periodontal pocket depth at distal buccal and distal lingual side of second molar

Secondary Outcomes

  • soft tissue healing index(7th postoperative day)

Study Sites (1)

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