Socket Preservation Using Socket-plug Technique With Alloplastic Putty Bone Versus Ice Cream Cone Technique in Extraction Socket With Buccal Dehiscence.

Not Applicable

Not yet recruiting

• Conditions: Socket Preservation

• Registration Number: NCT06655766
• Lead Sponsor: Cairo University

Brief Summary

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.

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 Timeline

• Study First Submitted: 2024-10-20
• Study First Submitted QC: 2024-10-22
• Study First Posted: 2024-10-23
• Status Verified: 2025-04
• Last Update Submitted: 2025-04-14
• Last Update Posted: 2025-04-17
• Study Start: 2025-04-30
• Primary Completion: 2025-11-13
• Study Completion: 2026-02-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 30

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 & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Quantitative volumetric changes	day 0 - month 6	Bone volumetric changes will be measured in millimeter by super-imposition of 3D scans using volume analysis software.

Secondary Outcome Measures

Name	Time	Method
Horizontal alveolar ridge width	day 0 - month 6	Buccolingual alveolar ridge width will be measured in millimeter 1, 3, 5 mm bellow alveolar crest in both groups.
Vertical alveolar ridge height	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.