Skip to content

Evaluation of Implant Placement by digital method

Evaluation of Placement Accuracy (Precision & Trueness) In Digitally-guided Implants and Prefabricated Provisional Single-unit Restorations: A Clinical Trial Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211208053334N1
Enrollment
14
Registered
2022-08-06
Start date
2022-08-11
Completion date
Unknown
Last updated
2022-08-29

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

Conditions

Partial loss of teeth, unspecified cause. Partial loss of teeth, unspecified cause

Interventions

Intervention group: single-unit implant placement in partially edentulous patients with the aid of surgical guides, which are designed (3shape dental system©) and printed after obtaining intraoral sca

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: at least two months after tooth extraction acceptable occlusion

Exclusion criteria

Exclusion criteria: presence of a systemic disease smoking contraindication for surgical procedures presence of parafunctional habits presence of TMJ complications need for graft or sinus lift surgery

Design outcomes

Primary

MeasureTime frame
The difference in implant angulation of designed and actual implants. Timepoint: immediately after surgery. Method of measurement: post-surgical CBCT.;The difference in apex location of designed and actual implants. Timepoint: immediately after surgery. Method of measurement: post-surgical CBCT.

Secondary

MeasureTime frame
The difference in placement angle of designed and actual crowns. Timepoint: two weeks after surgery and placement of the temporary restoration. Method of measurement: post-operative intraoral scanning.;The difference in crown depth of designed and actual crowns. Timepoint: two weeks after surgery and placement of the temporary restoration. Method of measurement: post-operative intraoral scanning.;Early Implant Failure. Timepoint: up to three months after surgery. Method of measurement: clinical and radiographic examination.;Bleeding on Probing. Timepoint: 3 months after surgery. Method of measurement: periodontal probing.;Peri-implant probing depth. Timepoint: 3 months after surgery. Method of measurement: periodontal probing.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactparsa pirooz

Tehran University of Medical Sciences

p-pirooz@student.tums.ac.ir+98 21 2200 7927

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 11, 2026