Immediate Implant Placementdental implantNCT06888947
Influence of Collagen Cone on the Outcomes of Immediate Dental Implant Placement in Esthetic Zone
An observational study of Immediate Implant Placement and Evaluate Buccal Bone Plate Around Dental Implant, run by Faculty of Dental Medicine for Girls at 1 site in Egypt.
Trial summary
Influence of Collagen Cone on the Outcomes of Immediate Dental Implant Placement in Esthetic zone Read more about this study
- Who is it for?
- Ages 30 to 50 years
- Conditions the study is for
- Immediate Implant Placement, Evaluate Buccal Bone Plate Around Dental Implant
- What is being tested?
- use immediate implant in socket with collagen cone
- Type of treatment
- Surgery or procedure
- How many people
- 16 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Apr 2024to 5 Aug 2026
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 30 to 50 years
- All sexes
- No healthy volunteers
- Adult
Study population: patient with unrestorable tooth/teeth in esthetic zone seeking tooth/teeth replacement.
Who may be able to join
- 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.
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
About this study
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.
- Being tested
- use immediate implant in socket with collagen cone
- Keywords
- immediate implant, collagen cone
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
use immediate implant in socket with collagen coneProcedure or surgery
use immediate implant in socket with collagen cone
| Study group | Role | What they receive |
|---|---|---|
| 8 patient will receive immediate implant with collagen cone. | 8 patient will receive immediate implant with collagen cone. Receives: 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. |
What is being measured
The primary outcome is the main question the study is designed to answer.
1- Clinical examination
Probing depth around the dental implant using graduated plastic periodontal probe (Keratinized Mucosa, bleeding on probing and gingival tissue condition)
Measured: 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.
Measured: 9 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Mar 2025
- Study start1 Apr 2024
- Primary completion2 Apr 2024
- Study completion5 Aug 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Immediate Implant PlacementStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Cross-sectional
- Enrolment
- 16 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Faculty of Dental Medicine for Girls
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Hala Fathy Abd El Fattah, Faculty of Dental Medicine for Girls
- Investigators
- Abeer Gawish, professor, Study director, Al-Azhar Universitylobna Abd-El Aziz, Lecturer, Study director, Al-Azhar University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06888947
- Sponsor's protocol ID
- 1445 AH - 2023 AG
- Other IDs
- 1234
- Acronym
- dental implant
- Status last verified
- Jan 2025
- First submitted
- 7 Jan 2025
- Last updated
- 21 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 21 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Influence of Collagen Cone on the Outcomes of Immediate Dental Implant Placement in Esthetic Zone
- ClinicalTrials.gov ID
- NCT06888947
- Acronym / sponsor ID
- dental implant / 1445 AH - 2023 AG
- Keywords
- immediate implant, collagen cone
- Study type
- Observational
- Recruitment status
- Enrolling by invitation
- Enrolment
- 16 participants (estimated)
- Lead sponsor
- Faculty of Dental Medicine for GirlsOther government
- Study start
- 1 Apr 2024 (actual)
- Primary completion
- 2 Apr 2024 (actual)
- Study completion
- 5 Aug 2026 (estimated)
- First posted
- 21 Mar 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Case-control
- Time perspective
- Cross-sectional
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 8 patient will receive immediate implant with collagen cone. | – | Procedure: use immediate implant in socket with collagen cone8 patient will receive immediate implant with collagen cone. |
| Control group 8 patient will receive immediate implant. | – | –Control group 8 patient will receive immediate implant. |
Who may qualify
- Ages
- 30 to 50 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- patient with unrestorable tooth/teeth in esthetic zone seeking tooth/teeth replacement.
Key inclusion criteria (2 listed)
- 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.
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| use immediate implant in socket with collagen coneuse immediate implant in socket with collagen cone | Procedure or surgery | 8 patient will receive immediate implant with collagen cone. |
Primary outcome
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)
1 secondary outcome
CBCT
Time frame: 9 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Mar 2025.
- Individual participant dataSharing planned: Undecided
Related trials for Immediate Implant Placement
Not yet recruiting
Effect of Customized Versus Stock Healing Abutments on Peri-Implant Soft Tissue
Peri-Implantitis
Enrolling by invitation
Peri-implant Tissue Changes Using Dual Zone Concept With Connective Tissue Graft Versus Concentrated Growth Factor
Hopeless Tooth in Esthetic Zone, Loss of Soft and Hard Tissue Around Implant
Active, not recruiting
The Aim of the Study Will be Clinically and Radio Graphically Comparison of Two Implant Designs Used to Treat Atrophied Mandible . Implant Design Comparison Will Done for Implant Stability,Peri-implant Soft Tissue Health Changes and Bone Changes .Patients Will be Divided Randomly Into Two Group
Dental Implant Bone Loss, Peri-Implant Health
Active, not recruiting
Healing Outcomes of Peri-implant Soft Tissues With Different Healing Abutments
Implant
Not yet recruiting
Impact of Intraoperative Neurotization on Sensory Recovery of the Nipple and Breast Skin in Patients Undergoing Nipple Sparing Mastectomy With Immediate Implant-Based Reconstruction: NERSENSE, Prospective Randomized Control Study
Breast Cancer
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Abeer Gawish, professor study director
Al-Azhar University
lobna Abd-El Aziz, Lecturer study director
Al-Azhar University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Immediate Implant Placement and Evaluate Buccal Bone Plate Around Dental Implant, run by Faculty of Dental Medicine for Girls at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: enrolling by invitation, as of the sponsor's last update on 21 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
1- Clinical examination (time frame: 9 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Mar 2025.