Influence of Collagen Cone on the Outcomes of Immediate Dental Implant Placement in Esthetic Zone (dental implant)

March 17, 2025 updated by: Hala Fathy Abd El Fattah, Faculty of Dental Medicine for Girls
Influence of Collagen Cone on the Outcomes of Immediate Dental Implant Placement in Esthetic zone

Study Overview

Status

Enrolling by invitation

Conditions

Intervention / Treatment

Detailed Description

The present study will be performed to assess effect of collagen cone for bone width and length around immediate implants in esthetics zone.

Study Type

Observational

Enrollment (Estimated)

16

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Egypt
      • Cairo, Egypt, 12345
        • Hala Fathy

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

patient with unrestorable tooth/teeth in esthetic zone seeking tooth/teeth replacement.

Description

Inclusion Criteria:

- 1-Patients were free from any systemic disease as evidenced by Burket's oral medicine health history questionnaire 2- Each patient required extraction of a non-restorable premolar or anterior tooth maxilla and requested implant restoration.

3-All patients should not have any known contraindication to oral surgery. 4-Male or female with age range 30 - 50 years.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
8 patient will receive immediate implant with collagen cone.
Procedure: use immediate implant in socket with collagen cone
use immediate implant in socket with collagen cone
Control group 8 patient will receive immediate implant.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
1- Clinical examination
Time Frame: 9 months
Probing depth around the dental implant using graduated plastic periodontal probe (Keratinized Mucosa, bleeding on probing and gingival tissue condition)
9 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
CBCT
Time Frame: 9 months
Improvement of esthetic outcome using collagen cone impacted in the socket with immediate implant by measure the improvement of bone width, length and density.
9 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Faculty of Dental Medicine for Girls

Investigators

  • Study Director: Abeer Gawish, professor, Azhar University
  • Study Director: lobna Abd-El Aziz, Lecturer, Azhar University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2024

Primary Completion (Actual)

April 2, 2024

Study Completion (Estimated)

August 5, 2026

Study Registration Dates

First Submitted

January 7, 2025

First Submitted That Met QC Criteria

March 17, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

March 17, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 1445 AH - 2023 AG
  • 1234 (Department of Defense)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Immediate Implant Placement

Clinical Trials on use immediate implant in socket with collagen cone

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Saint Lucia

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

Subscribe