Overview

The Effect of Systemic Antibiotics on Post-surgical Complications and Patient-centered Outcomes in Patients Undergoing Implant Surgery With Guided Bone Regeneration and Simultaneous Sinus Floor Elevation

Status:
Not yet recruiting
Trial end date:
2025-01-01
Target enrollment:
0
Participant gender:
All
Summary
The primary aim of the trial is to evaluate the effect of systemic antibiotic administration compared to placebo in patients undergoing oral implant therapy with simultaneous lateral sinus floor elevation and guided bone regeneration (GBR) in regard to patient-centered outcomes. The secondary aims of the trial is to evaluate the effect of systemic antibiotic administration on postsurgical complications, in patients undergoing oral implant therapy with simultaneous lateral approach sinus floor elevation and guided bone regeneration (GBR).
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Medical University of Graz
Treatments:
Amoxicillin
Criteria
Inclusion Criteria:

1. Medically healthy adult: ASA (American Society of Anesthesiologists) classification
I-II, age ≥ 21 years old

2. Non-smoker, previous smoker (quit ≥ 5 years); light smoker with less than 10
cigarettes/ day

3. Not allergic to Amoxicillin/Penicillin antibiotics, NSAIDS (Nonsteroidal
anti-inflammatory drugs) or corn-starch

4. Edentulous spaces in the posterior maxilla in one or 2 posterior quadrants with an
alveolar bone defect requiring sinus floor elevation and allowing implant placement of
up to 3 dental implants and simultaneous GBR (residual crest height 3-5 mm; per
implant site (Felice et al. 2012; Park et al. 2019).

5. Absence of signs of pathology of the sinus membrane and acute sinusitis requiring
ongoing management -

Exclusion Criteria:

1. Medically compromised subjects (ASA classification III-V)

2. General contraindications against implant treatment or augmentative procedures (e.g.
immunodeficiency, advanced systemic diseases, corticosteroid medication)

3. Those taking Bisphosphonates/anti-angiogenic/RANKL (Receptor activator of nuclear
factor kappa-Β Ligand) inhibitor medications or receiving local radio-therapy

4. Heavy smoker or previous heavy smoker (quit < 5 years; ≥ 10 cigarettes/day)

5. Allergic to Amoxicillin or Penicillin antibiotics, NSAIDS and / or corn starch

6. Use of any form of antibiotics in the last 3 months or subjects requiring regular
antibiotic prophylaxis prior to dental treatment

7. Pregnant or breast feeding. Self-declared intend to conceive (A pregnancy test will be
performed for all female patients).

8. Need for 2 stage sinus augmentation

9. Acute or unmanaged symptomatic sinusitis

10. Type 1 implant placement (immediate implant placement following extraction)

11. Need for simultaneous soft tissue augmentation

12. Residual bone height of > 5mm.

13. Subjects aged < 21 years old