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Clinical Trials/NCT06936358
NCT06936358CompletedNot Applicable

Comparison of the Effect of Injectable Platelet-rich Fibrin and Advanced Platelet-rich Fibrin With Xenograft on the Socket Preservation of Mandibular Extracted Molars ( a Randomised Controlled Clinical Trial) Comparison of the Effect of Injectable Platelet-rich Fibrin and Advanced Platelet-rich Fibrin With Xenograft on the Socket Preservation of Mandibular Extracted Molars ( a Randomised Controlled Clinical Trial)

Hams Hamed Abdelrahman1 site in 1 country16 target enrollmentStarted: August 22, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
16
Locations
1
Primary Endpoint
Change in healing

Study Overview

Brief Summary

Different materials and techniques are employed for socket preservation to reduce the alveolar bone resorption in both the horizontal and vertical dimensions as well as the soft tissue collapse after tooth extraction. Because of the repair abilities of the growth factors and proteins released by platelets, the development and application of platelet-enriched preparations have revolutionised the area of regenerative medicine.The present study will be designed to study the difference between A-PRF and IPRF with the addition of Xenograft in the preservation of bone in mandibular molars.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients who need extraction of hopeless mandibular molars
  • •Teeth with advanced caries not amenable for conservative treatment
  • •Patients who are willing and fully capable of complying with the study protocol.

Exclusion Criteria

  • •Systemic diseases that prevent surgery
  • •Acute or chronic oral infections
  • •Periodontal diseases
  • •Heavy smokers or alcoholics
  • •On anticoagulant drugs.
  • •Pregnancy
  • •History of radiotherapy or chemotherapy of the head and neck region

Arms & Interventions

Control

Active Comparator

Intervention: Control (Other)

A-PRF

Experimental

Intervention: A-PRF (Other)

I-PRF

Experimental

Intervention: I-PRF (Other)

Outcomes

Primary Outcomes

Change in healing

Time Frame: Baseline and 12 weeks

A modified Landry, Turnbull, and Howley healing index will be used to assess wound healing (HI). This entails evaluating the following parameters in a comparative manner using a dichotomic score (1/0). Tissue colour or the presence or absence of redness to indicate inflammatory processes; granulation tissue; suppuration; swelling; degree of tissue epithelialisation (partial or complete); and the presence or absence of bleeding and tenderness on palpation

change in bone density

Time Frame: Baseline and 12 weeks

Bone density will be measured using CBCT examinations

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Hams Hamed Abdelrahman
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Hams Hamed Abdelrahman

Lecturer of Dental Public Health and biostatistical consultanat

Alexandria University

Study Sites (1)

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