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Enrolling by invitation NCT06888947

Influence of Collagen Cone on the Outcomes of Immediate Dental Implant Placement in Esthetic Zone

— Observational Immediate Implant Placement Evaluate Buccal Bone Plate Around Dental Implant

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: use immediate implant in socket with collagen cone.
Who it may be relevant to
Registry conditions: Immediate Implant Placement, Evaluate Buccal Bone Plate Around Dental Implant. Basic parameters: 30 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

Influence of Collagen Cone on the Outcomes of Immediate Dental Implant Placement in Esthetic zone

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.

Interventions

  • Procedure use immediate implant in socket with collagen cone
    use immediate implant in socket with collagen cone

Primary outcome measures

  • 1- Clinical examination [Time frame: 9 months]
Secondary outcome measures (1)
  • CBCT [Time frame: 9 months]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-control

Study locations

Egypt · 1 center
  • Hala Fathy — Cairo

Identifiers

NCT: NCT06888947 · 1445 AH - 2023 AG · 1234

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗