Trials / Not Yet Recruiting
Not Yet RecruitingNCT07417293
Clinical and Patient Outcomes of 4 mm Ultra-Short vs. 8 mm Implants With Bone Augmentation in the Back Upper Jaw
Clinical- and Patient-related Outcomes of 4 mm Ultra-short Implants Compared to 8 Mm-long Implants With Bone Augmentation for the Rehabilitation of Posterior Atrophic Maxilla: a Randomized Controlled Clinical Trial.
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 35 (estimated)
- Sponsor
- Universitat Internacional de Catalunya · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study aims to compare 2 different groups of patients with both a healed site in the upper posterior sector after extractions, one treated with ultra-short implants, and another with long implants with bone regeneration. The objective is to evaluate if short-implants are superior in terms of better clinical outcomes, survival rates and safety, reduced surgical time, postoperative discomfort, and complication risk compared to conventional implants and bone regeneration.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Ultra short implants | Placement of an ultra short implant of 4mm in the posterior atrophic maxilla without any bone regeneration procedure |
| DEVICE | Long implants with bone augmentation | Placement of long implants of 8mm in the posterior atrophic maxilla alongside bone augmentation |
Timeline
- Start date
- 2026-02-20
- Primary completion
- 2028-07-01
- Completion
- 2029-07-01
- First posted
- 2026-02-18
- Last updated
- 2026-02-18
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT07417293. Inclusion in this directory is not an endorsement.