Immediately Placed Implant Sealed With Platelets Rich Fibrin Versus Cyanoacrylate Glue

H

Hams Hamed Abdelrahman

Status

Active, not recruiting

Conditions

Tooth Socket

Treatments

Other: Platelet-rich fibrin (PRF)
Other: Cyanoacrylate glue

Study type

Interventional

Funder types

Other

Identifiers

NCT05437744
Cyanoacrylates_2021

Details and patient eligibility

About

The health of peri-implant soft tissues is one of the most important aspects necessary for the long-term survival of dental implants. The importance of the peri-implant mucosal region lies in the need to establish a tight seal that isolates the implant and the bone from the oral environment. Study objective is to clinically compare the soft tissue healing, height, and thickness over immediate implants placed in type I sockets sealed by PRF to those sealed by a Cyanoacrylate glue.

Full description

the study will be conducted on 16 extraction sockets in humans. Sockets will be randomly divided into two groups: Group I (test) will comprise 8 sockets sealed by PRF after immediate implant placement. Group II: (test) will comprise 8 sockets sealed by cyanoacrylate glue after immediate implant placement

Enrollment

16 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Any non-restorable hopeless tooth; a badly decayed tooth that cannot be restored, a Tooth with failed endodontic treatment, and tooth with longitudinal fracture.
  • Post-extraction sockets type 1 with all bony walls intact; Type I extraction sockets according to Elian classification in 2007 have an intact labial plate of the bone and no soft tissue recession. Therefore, it does not require a mucoperiosteal flap elevation, only bone graft particles are packed into the socket after atraumatic extraction and socket debridement, then sealed with barrier membranes or soft tissue graft
  • A good standard of oral hygiene.
  • No signs of active periodontal disease in the selected tooth.

Exclusion criteria

  • The presence of any systemic disease that could complicate bone or soft tissue healing after immediate implant placement.
  • The presence of Acute periapical infection.
  • The presence of any local factor that may interfere with extraction as tooth ankyloses. (
  • Subjects who had undergone therapeutical radiation. (38)
  • Patients who had been subjected to or who were under bisphosphonate therapy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

16 participants in 2 patient groups

Study group
Experimental group
Treatment:
Other: Cyanoacrylate glue
Control group
Active Comparator group
Treatment:
Other: Platelet-rich fibrin (PRF)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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