Skip to content

Comparison of the effects of two different xenograft materials in implant surgery with maxillary sinus grafting.

Maxillary sinus graft by crestal approach simultaneously conducted with guided implant placement comparing collagenated soft-type block versus particulated bone substitute: A multicenter randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0010497
Enrollment
40
Registered
2025-05-22
Start date
2025-04-29
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

None listed

Interventions

None listed

Sponsors

Yonsei University Health System, Dental Hospital
Lead Sponsor
VHS Medical Center
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients aged 19 years or older who agree to participate in the clinical trial and have signed the informed consent form. 2. Sites in the posterior maxilla where more than 3 months have passed since tooth extraction. 3. Patients requiring maxillary sinus augmentation, in whom preoperative computed tomography shows 4–8 mm of vertical bone height at the edentulous site in the posterior maxilla, making them suitable candidates for a crestal approach to place implants of 8–10 mm in length. 4. Patients with no pathological findings in the maxillary sinus area.

Exclusion criteria

Exclusion criteria: 1.Patients with uncontrolled metabolic diseases (e.g., uncontrolled diabetes). 2.Individuals with a history of taking medications that may affect bone metabolism (e.g., bisphosphonates or denosumab) within the past 3 months. 3.Patients with uncontrolled gingivitis, periodontitis, or dental caries. 4.Patients with a history of tumor resection at the planned surgical site. 5.Individuals who have undergone chemotherapy or radiation therapy to the craniofacial region. 6.Heavy smokers consuming more than one pack (20 cigarettes) per day. 7.Pregnant or breastfeeding patients.

Design outcomes

Primary

MeasureTime frame
Three-dimensional evaluation of volumetric changes in the grafted maxillary sinus area over time

Secondary

MeasureTime frame
Two-dimensional evaluation of height changes in the grafted maxillary sinus area over time.;Evaluation of initial stability and osseointegration of the implanted implants.;Evaluation of alveolar ridge volume changes at the implant placement site.;Evaluation of patient and clinician satisfaction survey results.;Measurement of surgery duration.

Countries

Korea, Republic of

Contacts

Public ContactDAMI KIM

Yonsei University Health System, Dental Hospital

ekal7765@naver.com+82-2-2773-7765

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026