NCT06888947

Brief Summary

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

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
16

participants targeted

Target at below P25 for all trials

Timeline
3mo left

Started Apr 2024

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress90%
Apr 2024Aug 2026

Study Start

First participant enrolled

April 1, 2024

Completed
1 day until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 2, 2024

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

January 7, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

March 21, 2025

Completed
1.4 years until next milestone

Study Completion

Last participant's last visit for all outcomes

August 5, 2026

Expected
Last Updated

March 21, 2025

Status Verified

January 1, 2025

Enrollment Period

1 day

First QC Date

January 7, 2025

Last Update Submit

March 17, 2025

Conditions

Immediate Implant PlacementEvaluate Buccal Bone Plate Around Dental Implant

Keywords

immediate implantcollagen cone

Outcome Measures

Primary Outcomes (1)

  • 1- Clinical examination

    Probing depth around the dental implant using graduated plastic periodontal probe (Keratinized Mucosa, bleeding on probing and gingival tissue condition)

    9 months

Secondary Outcomes (1)

  • CBCT

    9 months

Study Arms (2)

8 patient will receive immediate implant with collagen cone.

8 patient will receive immediate implant with collagen cone.

Procedure: use immediate implant in socket with collagen cone

Control group 8 patient will receive immediate implant.

Control group 8 patient will receive immediate implant.

Interventions

use immediate implant in socket with collagen conePROCEDURE

use immediate implant in socket with collagen cone

8 patient will receive immediate implant with collagen cone.

Eligibility Criteria

Age30 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hala Fathy

Cairo, 12345, Egypt

Location

Study Officials

  • Abeer Gawish, professor

    Al-Azhar University

    STUDY DIRECTOR

  • lobna Abd-El Aziz, Lecturer

    Al-Azhar University

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

January 7, 2025

First Posted

March 21, 2025

Study Start

April 1, 2024

Primary Completion

April 2, 2024

Study Completion (Estimated)

August 5, 2026

Last Updated

March 21, 2025

Record last verified: 2025-01

Locations

EG(1)