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Randomized Clinical Study Comparing Two Guided Surgery Techniques for Free-end Implant Placement

Randomized Clinical Study Comparing Two Guided Surgery Techniques for Free-end Implant Placement: A Multicenter Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06764654
Enrollment
20
Registered
2025-01-08
Start date
2025-01-01
Completion date
2026-03-01
Last updated
2025-07-09

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

Conditions

Bone Resorption, Dental Implant

Keywords

guided suergery, dental implant, partial edentulous

Brief summary

This is a randomized multicenter clinical study that compares two static guided surgery techniques in free-end partial edentulism. The aim is to compare the accuracy obtained between dento-osseous supported and dento-mucosal supported surgical splints to place dental implants in posterior osseous ridges.

Interventions

PROCEDUREDental implant placement

Placement of two dental implants in the jaw.

Sponsors

Mozo Grau Ticare
CollaboratorUNKNOWN
Aula Dental Avanzada
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Masking description

The operator does not know what type of surgical splint to use until the very moment of the operation, just after the anesthesia is applied.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients who present to one of the two participating clinics with a posterior edentulous area starting from the second premolar. * Patients in whom the placement of dental implants is not contraindicated.

Exclusion criteria

* Patients with hypersensitivities or allergies that contraindicate the intervention. * Presence of orofacial neurological symptoms. * Patients treated with bisphosphonates. * Pregnant or breastfeeding women, or women undergoing contraceptive treatment. * Signs of infection in the surgical area. * Need for unconventional surgical procedures (e.g., split crest, vertical regeneration, block graft). * Lack of patient cooperation.

Design outcomes

Primary

MeasureTime frameDescription
Three-dimensional implant position deviations (measured by intraoral scan and planning software)From enrollment to the end of surgeryThree-dimensional deviations between the planned implant position and the actual postoperative implant position will be assessed. The deviations will be measured using an intraoral scanner (Medit i700®) and planning software (BlueSky Plan®). Units of measure: horizontal and vertical linear deviation (in millimeters), global deviation (in millimeters), and angular deviation (in degrees), evaluated at both implant entry and apex points.

Secondary

MeasureTime frameDescription
Three-dimensional implant position deviations (measured by CBCT and planning software)From enrollment to the end of surgeryThree-dimensional deviations between the planned implant position and the actual postoperative implant position will be assessed. The deviations will be measured using cone-beam computed tomography (CBCT) and planning software (BlueSky Plan®). Units of measure: horizontal and vertical linear deviation (in millimeters), global deviation (in millimeters), and angular deviation (in degrees), evaluated at both implant entry and apex points.

Countries

Spain

Contacts

Primary ContactGuillem Esteve-Pardo, PhD
guillem@clinicaesteve.es+34 965215755

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026