Investigating the effect of liquid PRF in maintaining dental socket

Not Applicable

Recruiting

• Conditions: Maintaining the socket dimensions of the tooth after tooth extraction for implant treatment.

• Registration Number: IRCT20221227056937N1
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

The patient must be over 18 years old
single root tooth that needs to be pulled and replaced with dental implant restoration.
Remaining bone support more than 50%

Exclusion Criteria

The presence of any systemic disease or disease that affects bone healing
Taking any medicine that is effective on bone healing
Existence of severe or uncontrolled systemic disease
Pregnancy
Daily consumption of 10 cigarettes or more
History of radiotherapy
Having a contraindication for implant placement
Using any prosthesis in the intervention site
Need for antibiotic prophylaxis
Presence of widespread infection near the intervention site

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Alveolar socket width: the width of the alveolar bone in the midbuccal region from the buccal side to the lingual side of the drawn tooth. Timepoint: At the beginning of the study (before the start of the intervention) and 3 months after the intended treatment. Method of measurement: The digital caliper calculates the width of the alveolar bone in the midbuccal area from the buccal to the lingual side of the extracted tooth with an accuracy of 0.01 mm.

Secondary Outcome Measures

Name	Time	Method
Radiographic evaluation. Timepoint: The beginning of the study (before the intervention) and 3 months after the intervention. Method of measurement: By using CBCT deviceThe alveolar socket is evaluated in the buccolingual and mesiodistal dimensions at 1, 3 and 5 mm sections.;Amount of vital bone. Timepoint: At the beginning of the study (before the start of the intervention) and 3 months after the intervention. Method of measurement: Presence of osteocyte and osteoblast along with bone trabeculae in bone tissue through light microscope evaluation.;Socket vertical height in the midbuccal region. Timepoint: At the beginning of the study (before the start of the intervention) and 3 months after the intervention. Method of measurement: The height of the alveolar bone in the midbuccal area from the CEJ of the adjacent tooth to the edge of the alvelar crest was measured with a digital calliper to the accuracy of 0.01 mm.