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Clinical and Radiographic Evaluation of Natural Bovine Bone With Hyaluronic Acid on Osseointegration of Immediate Implant.

Clinical and Radiographic Evaluation of Natural Bovine Bone With Hyaluronic Acid on Osseointegration of Immediate Implant: A Randomized Clinical Study

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07199725
Enrollment
16
Registered
2025-09-30
Start date
2022-11-08
Completion date
2023-05-20
Last updated
2025-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Implants

Keywords

immediate dental implants, natural bovine bone

Brief summary

the goal of this study is to evaluate the effective of natural bovine bone with hyaluronic acid on osseointegration of immediate implants in single rooted badly decayed maxillary anterior teeth and premolars. the main question it aims to answer is does natural bovine with hyaluronic acid affects osseointegration of immediate implants. the study compares immediate implants followed by grafting with natural bovine bone with hyaluronic acid to immediate implants without grafting.

Interventions

COMBINATION_PRODUCTimmediate dental implant

control group: 8 teeth were extracted then 8 immediate implants were placed without bone grafting

COMBINATION_PRODUCTimmediate dental implant, natural bovine bone substitute material

study group: 8 teeth were extracted then received 8 immediate implants followed by grafting with natural bovine bone substitute material with hyaluronic acid

Sponsors

Suez Canal University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

This clinical study was conducted on 16 badly decayed single rooted maxillary anterior teeth and premolars that received 16 immediate implants equally randomized divided into 2 groups. control group: 8 implants were inserted in 8 fresh extraction sockets study group: 8 implants were inserted in 8 fresh extraction sockets followed by grafting with natural bovine bone substitute material with hyaluronic acid (act as study group).

Eligibility

Sex/Gender
ALL
Age
21 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* medically free patients, good oral hygiene, no periapical lesions around teeth to be extracted

Exclusion criteria

* patients with bone or soft tissue defects, poor oral hygiene, heavy smoking, bruxism, severe periodontal disease

Design outcomes

Primary

MeasureTime frameDescription
Bone densitybaseline (immediately) and 6 monthsusing cone beam CT bone density was measured around the implant in housefield units immediately after implant placement and after 6 months.
implant stabilityBaseline (immediately) and after 4 monthsusing Osstell device, implant stability was measured immediately after implant placement and after 4 months

Secondary

MeasureTime frameDescription
Bone widthBaseline (immediately) and 6 monthsusing cone beam CT, buccal bone width was measured from the mid surface of the implant immediately after implant placement and after 6 months.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 8, 2026