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Clinical Trials/NCT04957654
NCT04957654
Unknown
N/A

A Comparative Study Evaluating Vestibular Socket Therapy in Immediate Implants Using Different Grafting Materials

Mohamed Mofreh Hamada Hamed1 site in 1 country24 target enrollmentMarch 16, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Tooth Extraction
Sponsor
Mohamed Mofreh Hamada Hamed
Enrollment
24
Locations
1
Primary Endpoint
changes in facial plate height
Last Updated
4 years ago

Overview

Brief Summary

The current research aims at evaluating the outcomes of the vestibular socket therapy in immediate implants using collagen plug, demineralized freeze-dried bone allograft, and deproteinized bovine bone minerals at both radiographic and clinical levels

Registry
clinicaltrials.gov
Start Date
March 16, 2021
End Date
July 1, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Mohamed Mofreh Hamada Hamed
Responsible Party
Sponsor Investigator
Principal Investigator

Mohamed Mofreh Hamada Hamed

clinical researcher

Tanta University

Eligibility Criteria

Inclusion Criteria

  • Patients will be included if they have one or more hopeless teeth without signs of acute infection in the maxillary anterior region.
  • Remaining roots or non-restorable teeth with sufficient bone apically and palatably to allow proper implant positioning with sufficient primary stability.
  • Optimal compliance as evidenced by no missed treatment appointments and a positive attitude towards oral hygiene.
  • Medically free

Exclusion Criteria

  • Medically compromised patients and systemic conditions precluding implant and periodontal surgery.
  • Smokers, diabetics, pregnant or lactating women.
  • History of chemotherapy, radiotherapy in head and/or neck region.
  • Bisphosphonate therapy

Outcomes

Primary Outcomes

changes in facial plate height

Time Frame: at baseline, 6 and 12 months

Each group will be subjected to: Cone beam computed tomography (CBCT) at baseline, 6 months, and 12months to assess height of labial (facial) plate of bone and implant survival

changes in facial plate thickness

Time Frame: at baseline, 6 and 12 months

Each group will be subjected to: Cone beam computed tomography (CBCT) at baseline, 6 months, and 12months to assess the thickness of the labial (facial) plate of bone and implant survival

Secondary Outcomes

  • changes in peri-implant mucosal level(at baseline, 3rd and 6th months)

Study Sites (1)

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