Immediate Restoration of a New Implant With High Primary Stability
Starting soon · Not applicable
Conditions studied: Dental Implants, Immediate Dental Implant Loading
In brief
The main objective of this scientific study is to evaluate the short-term (1-year) survival and success rates of dental implants restored immediately compared to implants restored after a three-month healing period. The total duration of the study is 12 months following implant placement, during which clinical and radiographic evaluations will be carried out at different follow-up time points.
Key facts
- Study ID
- NCT07498556
- Run by
- Universidade do Porto
- People needed
- 50
- Starts
- 2026-07-01
- Expected to finish
- 2027-12-30
- Last updated by the study team
- 2026-05-05
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Men and women between 18 and 70 years of age.
- Ability to read, understand, and sign the informed consent form.
- Need for placement of one or more implants for fixed prosthetic rehabilitation in either arch.
- Insertion torque ≥ 35 Ncm (lower values will be excluded from the study).
- Adequate bone dimensions to receive an implant with diameter ≥ 3.75 mm and length ≥ 10 mm.
- Bone type I to III at the insertion site.
- Good oral hygiene: FMBS and FMPS ≤ 25%.
- Systemic status classified as ASA I or II.
You may not qualify if…
- Inability to attend follow-up appointments.
- Systemic contraindications to oral surgery (ASA III or IV).
- Pregnancy or breastfeeding.
- Chronic use of corticosteroids, bisphosphonates, or RANKL inhibitors within the last year.
- Alcohol or drug abuse.
- Heavy smoking (≥ 10 cigarettes/day).
- Previous radiotherapy in the cervicofacial region.
- Untreated active periodontal disease.
- Absence of antagonist teeth.
- Local pathology at the planned implant site.
- Uncontrolled diabetes mellitus (HbA1c > 7%).
- Bone type IV at the surgical site.
Where it is running
- Faculdade De Medicina Dentaria da Universidade do Porto — Porto, Portugal
Full record on ClinicalTrials.gov
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