Surface Treatment of the Dental Implant on the Osseointegration

NCT ID: NCT05194813

Last Updated: 2022-01-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-11-01
• Study Completion Date: 2021-06-15

Brief Summary

Dental implants have become a widely accepted treatment modality for the replacement of missing single or multiple teeth in the recent years. In order to meet patients' needs for shorter treatment times and the necessity of dealing with more challenging clinical situations, implants and implant therapies have undergone continuous improvement to improve the function and longevity of the implants. Recently the constant search for improvements in modern implant have been focused on surface modifications so a new era of surface treatment have been showed up; the chemically modified hydrophilic surfaces.

Conditions

Dental Implants; Surface Treatment

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Hydrophilic sandblasted and acid-etched dental implants

Group Type: EXPERIMENTAL

Aqua alvim CM, neodent implant (Test)

Intervention Type: OTHER

Acqua, Hydrophilic sandblasted, and acid-etched dental implants

Conventional hydrophobic sandblasted and acid-etched dental implant

Group Type: ACTIVE_COMPARATOR

Neoporous alvim CM, neodent implant (Control)

Intervention Type: OTHER

Neoporous, Hydrophilic sandblasted, and acid-etched dental implants

Interventions

Aqua alvim CM, neodent implant (Test)

Acqua, Hydrophilic sandblasted, and acid-etched dental implants

Intervention Type: OTHER

Neoporous alvim CM, neodent implant (Control)

Neoporous, Hydrophilic sandblasted, and acid-etched dental implants

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Missing mandibular posterior teeth.
• Good oral hygiene (plaque index less than 10 %)
• Good compliance to the treatment.
• Participants are free from local or systemic disease
• Willingness and ability to commit to follow-up placement.
• Adequate bone height and width to accommodate implant placement and sufficient keratinzed mucosa.
• At least 3months after tooth extraction
• Sufficient interocclusal distance

Exclusion Criteria

• Presence of persistent and unresolved infection in the implant site
• Parafunctional habits.
• Heavy Smokers.
• Uncontrolled systemic disease that impedes bone healing

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hams Hamed Abdelrahman

OTHER

Sponsor Role: lead

Responsible Party

Hams Hamed Abdelrahman

Assistant lecturer of DPH and Clinical statistician

Responsibility Role: SPONSOR_INVESTIGATOR

Locations

Alexandria Faculty of Dentistry

Alexandria, , Egypt

Countries

Egypt

Other Identifiers

Implants2022

Identifier Type: -

Identifier Source: org_study_id