Clinical Trials Directory

Trials / Unknown

UnknownNCT05211362

Sticky Bone and Repeated Injectable PRF (iPRF) Application in Management of Periodontal Intrabony Defects

Sticky Bone and Repeated Injectable PRF Application in Management of Periodontal Intrabony Defects (Randomized Clinical Trial)

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
32 (estimated)
Sponsor
Al-Azhar University · Academic / Other
Sex
All
Age
18 Years – 48 Years
Healthy volunteers
Accepted

Summary

One of the main objectives of periodontal therapy is the regeneration of the tooth's supporting periodontal tissue to its original levels. The healing after non-surgical and conventional surgical methods is histologically characterized by a long junctional epithelium along the root surfaces. Therefore, reconstructive techniques are required. Although complete periodontal regeneration is unpredictable with any regenerative therapy currently used, so the objective of our trial is to get complete periodontal regeneration by using Sticky Bone and Repeated Injectable PRF (iPRF) in Management of Periodontal Intrabony Defects.

Conditions

Interventions

TypeNameDescription
BIOLOGICALSticky Bone and Repeated Injectable PRF (iPRF)The surgical treatment phase was initiated only if the subjects had a full-mouth dental plaque score of less than one and a test site plaque score of 0. Following mucoperiosteal flap reflection for one tooth on either side of the defect, all granulation tissue was removed from the defects by means of Gracey 7/8 metal curettes, and root surfaces were scaled and planed using hand and ultrasonic instruments, then the defect was filled with xenograft mixed with IPRF, Finally, the flap was replaced and closed with crossed horizontal and vertical internal mattress sutures.
BIOLOGICALbone substituteThe surgical treatment phase was initiated only if the subjects had a full-mouth dental plaque score of less than one and a test site plaque score of 0. Following mucoperiosteal flap reflection for one tooth on either side of the defect, all granulation tissue was removed from the defects by means of Gracey 7/8 metal curettes, and root surfaces were scaled and planed using hand and ultrasonic instruments, bone graft substitute was heavily condensed into the intra bony defects. The flap was replaced and closed with crossed horizontal and vertical internal mattress sutures.

Timeline

Start date
2022-04-16
Primary completion
2022-08-25
Completion
2022-11-22
First posted
2022-01-27
Last updated
2022-03-08

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05211362. Inclusion in this directory is not an endorsement.