Endoscopic-Assisted Versus Conventional Crestal Sinus Lift
sinus lift
Clinical and Radiographic Evaluation of Endoscopic-Assisted Versus Conventional Crestal Sinus Lift: A Randomized Controlled Clinical Trial
1 other identifier
interventional
24
1 country
1
Brief Summary
To compare Endoscopic-Assisted Versus Conventional Crestal Sinus Lift; bone grafting will be performed, followed by implant placement. Membrane perforation rates, surgical time, and bone density changes will be evaluated.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 25, 2026
CompletedFirst Submitted
Initial submission to the registry
September 11, 2026
CompletedFirst Posted
Study publicly available on registry
September 17, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 31, 2028
September 17, 2026
May 1, 2026
2 years
September 11, 2026
September 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Membrane integrity intraoperative.
Membrane remains intact ( no perforation)
24 hours
Secondary Outcomes (1)
mean bone density
6 months
Study Arms (2)
Endoscopic-guided sinus lift
EXPERIMENTALEndoscopic-guided sinus lifting
non-endoscopic-guided sinus lift
PLACEBO COMPARATORconventional sinus lift
Interventions
12 patients in Group 2 (Endoscopic-guided): Endoscopic evaluation was conducted after each drilling step, osteotome malleting, and bone graft placement to monitor sinus membrane integrity.
12 patients in Group 1(non-endoscopic-guided): Endoscopic evaluation was performed after complete osteotomy preparation and sinus membrane elevation using osteotomes.
Eligibility Criteria
You may qualify if:
- Loss of one or more maxillary posterior tooth, Patients age≥21 years, Bone height was 4-7 mm, sufficient inter-arch space and mesio-distal width.
You may not qualify if:
- Parafunctional habits, Drug or alcohol abuse, uncontrolled systemic diseases that contraindicate implant surgery, pregnant women, Smokers.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Nahla Mahmoud Awadlead
- Cairo Universitycollaborator
Study Sites (1)
Cairo University
Cairo, Cairo Governorate, 12515, Egypt
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- associate professor of oral and maxillofacial surgery
Study Record Dates
First Submitted
September 11, 2026
First Posted
September 17, 2026
Study Start
May 25, 2026
Primary Completion (Estimated)
May 31, 2028
Study Completion (Estimated)
July 31, 2028
Last Updated
September 17, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share