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CompletedNCT07840339G-PTERYGOIDUpdated Sep 25, 2026

Guided Pterygoid Implants: an Accuracy Study

An interventional study of 3D Printed Digital Surgical Guide in Atrophic Posterior Maxilla, sponsored by Tanta University. Completed at 1 site in Egypt. Open to participants aged 20 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-09-25.

Sponsored by Tanta University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
9
Allocation
Not applicable
Ages
20 Years to 60 Years
Sex
All
01

Study summary

The aim of this clinical study is to evaluate the accuracy of placing pterygoid implants using custom-made surgical guides in patients with atrophied posterior maxilla. The study focuses on measuring how closely the actual implant position matches the virtual preoperative plan in terms of angle and distance.

Read the detailed description

Rehabilitation of the atrophic posterior maxilla remains a surgical challenge. This study utilizes pterygoid implants as a graftless solution. For each participant, a digital workflow is followed: a cone-beam computed tomography (CBCT) scan and an intraoral scan are performed to design a custom-made surgical guide. Following implant placement, a postoperative CBCT is obtained. The accuracy is then evaluated by superimposing the planned and actual implant positions to calculate the coronal, apical, and angular deviations.

02

Conditions studied

  • Atrophic Posterior Maxilla

Keywords

  • Bone support vs mucosa support
  • Pterygoid implant
  • Accuracy of the surgical guide
  • Computer-Aided Design
03

Who can participate

Ages eligible
20 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

-

The patients recruited for the study were selected according to the following criteria:

  • The age of the patients is between 20-60 years.
  • Partially and completely maxillary edentulous patients whose sinus pneumatization and refuse other treatment options.
  • Bone height related to the sinus is less than 5 mm.

Exclusion criteria

Exclusion Criteria:

  1. Prior radiation therapy
  2. Soft and hard tissue pathology at the operation site • Systemically:

1. Patients with uncontrolled systemic disease 2. Previous chemotherapy and/or antiresorptive agents 3. Heavy smoking (e.g., two packs per day)

04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
9 participants (actual)

Study arms

  • Experimental
    Guided Pterygoid Implant

    Patients with atrophic posterior maxilla receiving pterygoid implants using a custom-made digital surgical guide to evaluate placement accuracy.

    Device: 3D Printed Digital Surgical Guide

Interventions

  • Device3D Printed Digital Surgical Guide

    A custom-made surgical template designed using technology based on the patient's CBCT and intraoral scans. It is used to guide the surgical drills and the placement of pterygoid implants according to a pre-planned virtual position to ensure accuracy

05

What researchers measure

Primary outcomes

  1. Accuracy of custam made surgical guide

    Evaluation of the deviation between the virtual preoperative plan and the actual postoperative implant position. This includes angular and linear deviation

    Time frame: Immediately postoperative

06

Study locations

1 site
  • (Faculty of Dentistry - Tanta University
    Tanta, Gharbia Governorate 35111, Egypt
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07840339
Lead sponsor
Tanta University
Responsible party
Abdallah ahmed fathi gomaa (MSCs researcher, Tanta University) — Principal investigator
First posted
Sep 25, 2026
Start date
Aug 22, 2024
Primary completion
Aug 8, 2025
Completion
Apr 10, 2026
Last update
Sep 25, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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