- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06655766
Socket Preservation Using Socket-plug Technique With Alloplastic Putty Bone Versus Ice Cream Cone Technique in Extraction Socket With Buccal Dehiscence.
September 20, 2025 updated by: Abdelrahman Medhat, Cairo University
Socket Preservation Using Socket-plug Technique With Alloplastic Putty Bone Versus Ice Cream Cone Technique in Extraction Socket With Buccal Dehiscence: A Randomized Controlled Clinical Trial.
Socket Preservation Using Socket-plug Technique with Alloplastic Putty Bone Versus Ice Cream Cone Technique in Extraction Socket with Buccal Dehiscence: A Randomized Controlled Clinical Trial.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
this randomized controlled clinical trial evaluates the effect of using alloplastic putty bone with socket-plug technique versus ice-cream cone technique regarding dimensional changes in bone width
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Abdelrahman Medhat
- Phone Number: 01117909725
- Email: abdelrahman.medhat@dentistry.cu.edu.eg
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Single or double rooted teeth indicated for extraction.
- Systemically free patient
- Presence of small buccal dehiscence not exceeding 1/3 of the root.
- Maxillary and Mandibular Arches
- Non-smoker
- Adults or above the age of 21.
- Able to tolerate surgical periodontal procedures.
- Full mouth plaque and bleeding scores less than 15%.
- Compliance with the maintenance program.
- Provide informed consent
Exclusion Criteria:
- Systemic conditions/disease that contraindicate surgical procedure.
- Patients with presence or history of osteonecrosis of the jaws, with use of bisphosphonates, exposure to head and neck radiation, chemotherapy.
- Extraction socket with intact walls with no buccal dehiscence
- Patients with large distinct pre-apical pathology
- Heavy Smokers more than 10 cigarettes a day
- Patients without availability to attend follow-up visits or patients rejecting to sign the informed consent.
- Patients with parafunctional habits that produce overload on implant, such as bruxism and clenching.
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
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Socket-plug technique with putty bone
|
|
|
Active Comparator: Ice cream cone technique
|
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quantitative volumetric changes
Time Frame: day 0 - month 6
|
Bone volumetric changes will be measured in millimeter by super-imposition of 3D scans using volume analysis software.
|
day 0 - month 6
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Horizontal alveolar ridge width
Time Frame: day 0 - month 6
|
Buccolingual alveolar ridge width will be measured in millimeter 1, 3, 5 mm bellow alveolar crest in both groups.
|
day 0 - month 6
|
|
Vertical alveolar ridge height
Time Frame: day 0 - month 6
|
Vertical alveolar ridge height will be measured in millimeter from the end of the socket to the alveolar crest in both groups.
|
day 0 - month 6
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
October 30, 2025
Primary Completion (Estimated)
November 13, 2025
Study Completion (Estimated)
February 1, 2026
Study Registration Dates
First Submitted
October 20, 2024
First Submitted That Met QC Criteria
October 22, 2024
First Posted (Actual)
October 23, 2024
Study Record Updates
Last Update Posted (Estimated)
September 23, 2025
Last Update Submitted That Met QC Criteria
September 20, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- PER6-3-1 ..
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.
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