Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
COMPLETED
NCT07835451
NA

Effect of Bone Graft Material ON Peri-Implant Phenotype .

Sponsor: Al-Mustansiriyah University

View on ClinicalTrials.gov

Summary

This prospective three-arm controlled interventional clinical study evaluates the effects of NanoBone alone and NanoBone combined with platelet-rich fibrin (PRF) on peri-implant hard and soft tissue phenotype after dental implant placement. Thirty-nine adult participants requiring dental implant therapy will be assigned to three groups of 13 using a repeating sequential 1-2-3 allocation sequence: implant placement alone (control), implant placement with NanoBone, or implant placement with NanoBone and PRF/CGF membrane. Clinical and radiographic outcomes will be assessed at baseline, immediately after surgery, 8 weeks after surgery, and 4 months after surgery, with an early postoperative assessment of pain, swelling, medication use, and wound healing.

Official title: Evaluation of the Effect of Bone Graft Materials on Peri-Implant Phenotype: A Prospective Three-Arm Controlled Interventional Clinical Study

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

39

Start Date

2026-07-02

Completion Date

2026-09-01

Last Updated

2026-09-23

Healthy Volunteers

Yes

Conditions

Interventions

PROCEDURE

Dental implant placement

Dental implant placement without adding bone graft material or bone substitute at the implant site, according to the study protocol.

OTHER

NanoBone

Application of NanoBone at the implant site during dental implant placement.

OTHER

NanoBone sticky bone plus CGF/PRF membrane

Application of NanoBone sticky bone combined with a CGF/PRF membrane at the implant site during dental implant placement.

Locations (1)

Mustansiriyah University - College of Dentistry

Baghdad, Iraq