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Enrolling by invitationNCT06888947dental implantUpdated Mar 21, 2025

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

An observational study in Immediate Implant Placement and Evaluate Buccal Bone Plate Around Dental Implant, sponsored by Faculty of Dental Medicine for Girls. Enrolling by invitation at 1 site in Egypt. Open to participants aged 30 Years to 50 Years. Per ClinicalTrials.gov, last updated 2025-03-21.

Sponsored by Faculty of Dental Medicine for Girls · Observational

Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
16
Ages
30 Years to 50 Years
Sex
All
01

Study summary

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

Read the 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.

02

Conditions studied

  • Immediate Implant Placement
  • Evaluate Buccal Bone Plate Around Dental Implant

Keywords

  • immediate implant
  • collagen cone
03

In context

Lead sponsor

Faculty of Dental Medicine for Girls is the lead sponsor of 54 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

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

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 to oral surgery. 4-Male or female with age range 30 - 50 years.

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
16 participants (estimated)
Patient registry
No

Groups and cohorts

  • 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

  • Procedureuse immediate implant in socket with collagen cone

    use immediate implant in socket with collagen cone

06

What researchers measure

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)

    Time frame: 9 months

Secondary outcomes

  1. CBCT

    Improvement of esthetic outcome using collagen cone impacted in the socket with immediate implant by measure the improvement of bone width, length and density.

    Time frame: 9 months

07

Study locations

1 site
  • Hala Fathy
    Cairo, 12345, Egypt
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Apr 2024 to primary completion in Apr 2024, 0 months.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 7, 2025
First posted
Mar 21, 2025
StartActual
Apr 1, 2024
Primary completionActual
Apr 2, 2024
CompletionEst.
Aug 5, 2026
Last update
Mar 21, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 21, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06888947
Lead sponsor
Faculty of Dental Medicine for Girls
Responsible party
Hala Fathy Abd El Fattah (principal investigator, Faculty of Dental Medicine for Girls) — Principal investigator
First posted
Mar 21, 2025
Start date
Apr 1, 2024
Primary completion
Apr 2, 2024
Completion
Aug 5, 2026 (estimated)
Last update
Mar 21, 2025

Study contacts

Abeer Gawish, professor
study director · Al-Azhar University
lobna Abd-El Aziz, Lecturer
study director · Al-Azhar University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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