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NCT05403099 Clinical Trial

Effect of Topical Application of Hyaluronic Acid on Stability of Immediate Loading Dental Implant in Posterior Maxilla

Missing Teeth Clinical Trial

Official title:
Effect of Topical Application of Hyaluronic Acid on Stability of Immediate Loading Dental Implant in Posterior Maxilla

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05403099
Other study ID # 01010119
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2019
Est. completion date March 1, 2020

Study information
Verified date May 2022
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Effect of Topical Application of Hyaluronic Acid on Stability of Immediate Loading Dental Implant in Posterior Maxilla

Description:

Patients were randomly divided into two groups: Group I (Control group): Ten implants were placed in posterior maxilla and immediately loaded. Group II (Study group): Ten implants were coated with HA before placement in posterior maxilla and immediately loaded.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date March 1, 2020
Est. primary completion date March 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria: - Highly motivated patients with good oral hygiene. - Age 18 years or older. - Adequate alveolar bone volume at the implant site, at least 6mm in width and 15 mm in height. - Free from any parafunctional habits Exclusion Criteria: - Patients suffering from any systemic or local disease that contraindicate implant placement or surgery. - Pregnancy. - Smokers.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Hyaluronic acid
immediate placement of dental implant after topical application of hyaluronic acid on implant surface
• conventional implant placement
immediate placement of dental implant without application of hyaluronic acid on implant surface

Locations
Country Name City State
Egypt Merna Elhadidi Mansoura

Sponsors (1)
Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary implant stability using radiofrequency analysis immediately after surgery
Primary implant stability using radiofrequency analysis one month
Primary implant stability using radiofrequency analysis three months
Primary implant stability using radiofrequency analysis six months
Primary bone density bone density around the implant is measured in cone beam computed tomography three months
Secondary propping depth The distance between the gingival margin and the base of the pocket six months
Secondary bleeding inex Modified sulcus bleeding index six months
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