Clinical Trial

Impact of Hyaluronic Acid and Bone Graft on Peri-Implant Tissue

Completed
View on ClinicalTrials.gov →
Summary
This randomized controlled clinical trial aims to evaluate the effect of hyaluronic acid (HA) and particulate bone graft on the peri-implant tissue phenotype in patients receiving dental implants. Healthy adult participants requiring dental implant placement will be randomly allocated into one of three equal groups (12 implants per group): Group 1 will receive dental implants combined with hyaluronic acid gel (Gengigel); Group 2 will receive dental implants combined with both hyaluronic acid and particulate bone graft; and the control group will receive dental implants alone. Clinical and radiographic assessments will be performed using a customized measurement stent to ensure standardized evaluations at baseline, immediately postoperatively, and at 8 and 16 weeks of follow-up. The primary and secondary outcomes include alterations in ridge width, keratinized tissue width/thickness, radiographic soft tissue height, and marginal bone height. The study aims to determine whether the adjunctive use of hyaluronic acid and bone grafts enhances the quality of the peri-implant soft and hard tissue phenotype.
Protocol Amendment History 3 changes
critical Trial completed 2026-07-08
notable Primary completion pushed: 2026-06 -> 2026-07-02 2026-07-08
notable Primary completion moved earlier: 2026-07 -> 2026-06 2026-06-30
Trial Details
NCT Number NCT07665281
Lead Sponsor Al-Mustansiriyah University
Conditions Alveolar Bone Loss, Partially Edentulous Jaw, Dental Implant
Enrollment 36 participants
Start Date 2025-12-05
Primary Completion 2026-07-02 (estimated)
Study Completion 2026-07-02 (estimated)
Updated on ClinicalTrials.gov 2026-07-07