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Bone Augmentation of a Trephine/osteotome Maxillary Sinus Augmentation Approach: a Randomized Controlled Study

Bone Augmentation of a Trephine/osteotome Maxillary Sinus Augmentation Approach: a Randomized Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120875
Enrollment
Unknown
Registered
2026-03-20
Start date
2021-06-22
Completion date
Unknown
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dentition Defect

Interventions

The inlay osteotome sinus augmentation group:the inlay osteotome sinus augmentation
Conventional transalveolar sinus floor elevation group:conventional transalveolar sinus floor elevation

Sponsors

Hospital of Stomatology, Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Residual bone height (RBH) in the posterior maxilla is 4-6 mm. 2. Maxillary sinus floor exhibits a flat morphology without significant slopes or septa. 3. Presence of opposing dentition or prosthetic restoration. 4. Absence of maxillary sinusitis. 5. Adequate healing of the extraction socket with 4 months post-extraction. 6. Patients who voluntarily participated after providing written informed consent and complied with scheduled follow-ups.

Exclusion criteria

Exclusion criteria: 1. Uncontrolled systemic diseases (e.g., diabetes, immune disorders) 2. History of head and neck radiotherapy within one year 3. History of chemotherapy within one year 4. Uncontrolled periodontitis with unwillingness to receive periodontal treatment 5. Active or chronic maxillary sinus infections 6. Long-term smoking (>20 cigarettes/day) 7. Psychological disorders (e.g., depression, anxiety) compromising treatment cooperation 8. Declined scheduled post-treatment follow-ups 9. Pregnancy, lactation, or planned pregnancy within 2 years

Design outcomes

Primary

MeasureTime frame
linear bone augmentation;

Secondary

MeasureTime frame
Bone Gain Volume;Postoperative Pain Scores;Operative Time;

Countries

China

Contacts

Public ContactBin Shi

Hospital of Stomatology, Wuhan University

shibin_dentist@whu.edu.cn+86 138 0864 3395

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026