Skip to content

Evaluation of different time frames for prosthesis placement following dental implantation

Early loading in Implant Dentistry involving single prostheses: randomized controlled clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6ww3q3j
Enrollment
120
Registered
2026-03-18
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Jaw, Edentulous, Partially Jaw, Edentulous

Interventions

This is a randomized, open-label, four-arm controlled clinical trial that will evaluate the benefits of early loading in implant dentistry through clinical and radiographic examinations, as well as qu

Sponsors

Faculdade de Odontologia do Campus de Araçatuba - UNESP
Lead Sponsor
FGM Dental Group
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients of both genders; over 18 years of age; with good oral hygiene; no systemic contraindications for oral surgical therapy; with missing teeth or teeth indicated for extraction due to root fracture, caries, endodontic injury, or periodontal disease; who have an indication for rehabilitation with single implants; and who have adequate bone volume for implant placement, as assessed by Cone Beam Computed Tomography (bone availability for implants of at least 8 mm in length and 3.3 mm in diameter and without fenestrations in any wall that cannot be circumvented during surgery)

Exclusion criteria

Exclusion criteria: Totally edentulous patients; patients who use medication that contraindicates the installation of implants or may alter osseointegration; patients with uncontrolled underlying diseases; patients who do not have adequate bone volume for the installation of implants; post-extraction cases that require gap closure with biomaterial and/or the use of a membrane; pregnant or lactating women; and heavy smokers (more than 2 packs of cigarettes per day)

Design outcomes

Primary

MeasureTime frame
It's expected to evaluate whether implant placement and loading at different clinical times after surgery result in similar peri-implant bone changes throughout follow-up

Secondary

MeasureTime frame
It is expected to compare the level of pain, discomfort, and mood measured by Visual Analog Scale (VAS), in addition to the perception of improved oral health, assessing whether this perception is higher in groups with earlier implant activation

Countries

BR

Contacts

Public ContactFellippo Verri

Faculdade de Odontologia do Campus de Araçatuba - Universidade Estadual Paulista

fellippo.verri@unesp.br+55 (18) 3636-3308

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Apr 4, 2026