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Clinical Trials in Egypt / NCT07670559
Active, not recruiting Not applicable

Carrot Technique Versus Guided Bone Regeneration for Horizontal Ridge Deficiency in the Maxillary Esthetic Zone

NCT07670559 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-08-02
Last updated
2026-06-26

Condition(s) studied

Horizontal Alveolar Ridge DeficiencyPartial Edentulism

Investigational drug(s) / intervention(s)

Carrot TechniqueGuided Bone Regeneration

Carrot Technique: Implant placement with simultaneous horizontal ridge augmentation using an autogenous bone core harvested from the implant osteotomy site with a trephine drill and fixed buccally using osteosynthesis screws.

Guided Bone Regeneration: Implant placement with simultaneous horizontal ridge augmentation using bone substitute material and a collagen membrane according to guided bone regeneration principles.

Study summary

This randomized controlled clinical trial aims to compare the effectiveness of the Carrot Technique and Guided Bone Regeneration (GBR) for the management of horizontal alveolar ridge deficiency in patients requiring implant placement in the maxillary esthetic zone. Twenty patients will be randomly allocated into two equal groups. Clinical outcomes including implant stability and soft tissue healing, as well as radiographic outcomes including alveolar ridge width, bone density, and marginal bone loss, will be evaluated using clinical examinations and cone beam computed tomography (CBCT) during a 12-month follow-up period..

Eligibility

Sex
ALL
Min age
18 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged 18 to 45 years. Missing a single tooth in the maxillary esthetic zone requiring implant placement. Good oral hygiene and patient compliance. Medically free from systemic diseases that contraindicate implant surgery. Slight to moderate horizontal alveolar ridge deficiency with a minimum ridge width of 5 mm. Adequate vertical bone height for implant placement. Medium to hard bone quality (D2-D3 according to Misch classification). Absence of bruxism or other parafunctional habits. Exclusion Criteria: * Presence of local pathological lesions (e.g., cysts or tumors) at the planned surgical site. Poor bone quality (D4 bone). Pregnancy. Heavy smoking. Any medical condition contraindicating implant surgery.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Faculty of Dentistry, Mansoura University Al Mansurah Dakahlia Governorate
Faculty of Dentistry, Mansoura University Al Mansurah Egypt

More Mansoura University trials in Egypt

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07670559 on ClinicalTrials.gov ↗ ← All trials in Egypt