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CompletedNCT06400277Updated May 6, 2024

In-Vivo Comparison of Different Impression Methods in Complete Edentulous Upper Jaw

An interventional study of Edentulous maxilla final impression for complete denture in Edentulous Jaw, sponsored by Hacettepe University. Completed at 1 site in Turkey (Türkiye). Per ClinicalTrials.gov, last updated 2024-05-06.

Sponsored by Hacettepe University · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 1 year 8 months after the study started (first participant enrolled Jul 2022, registered Apr 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Non-randomized
Sex
All
01

Study summary

In this study, it was aimed to compare the impressions taken with different impression techniques for the production of tissue-supported complete dentures from individuals with complete edentulous upper jaws. For this purpose, 15 individuals with complete edentulism in the upper jaw were asked to participate in the study. In addition to agreeing to participate in the study after reading the consent form, these individuals should have been using tissue-supported complete dentures in the upper jaw for at least 3 months. They should also have healthy mucosa without local factors such as tissue hyperplasia, atrophic crests, allergic reaction, epulis fissuratum. A total of five final impressions will then be taken from these individuals in two sessions. Two of these impressions will be obtained with the traditional method and three with the digital method. The traditional impression group will include one-step (ALG) and two-step (ZOE) impression techniques. The digital impression group will include the digital impression taken when the artificial intelligence is deactivated (A.I OFF), the digital impression taken when the artificial intelligence is activated (A.I ON) and the modified technique (MOD). In the first appointment, the first impressions will be taken for the traditional and digital groups. Intraoral exclusion and isolation will be provided before the digital first impression. With the A.I mode of the intraoral scanner (TRIOS4; 3Shape A/S, Copenhagen, Denmark) deactivated, scanning will be performed in accordance with the scanning protocol recommended by the company. A metal stock tray suitable for the dental arch will then be selected for the preliminary impression of the traditional impression group. The impression will be taken in one step with irreversible hydrocolloid impression material. The impression will be digitized with the same intraoral scanner within the first 10 minutes after impression taking. Both impressions will be digitally transferred to the dental laboratory as stl data. Using computer aided design (CAD) software (Exocad DentalCAD 2.4 Plovdiv), an individual tray will be designed for the ZOE impression in the traditional group and a pedestal for the MOD impression in the digital impression group. The designs will be transferred to the computer aided manufacturing (CAM) unit and produced with a 3D printer using dental resin. The occlusal-rim (OR) will be prepared by adding wax on the base.

In the second appointment, the cheek and lips will be excluded in the same way before scanning. For A.I OFF and A.I ON, recordings will be taken when the artificial intelligence is deactivated and activated, respectively. Then, occlusal vertical dimension, intermaxillary relationship and aesthetic parameters will be determined with OR before scanning for the MOD group. Reference areas will be created on the buccal and palatinal walls to facilitate scanning of the OR. To avoid retention problems during scanning, a silicone-based impression material with a fluid consistency will be applied to the tissue surface of the OR and placed in the mouth. Scanning will be performed according to the protocol proposed by Lo Russo et al. For the traditional impression group, the ALG impression will be taken with a metal stock tray using irreversible hydrocolloid impression material in a single step. The impression will be digitized with an intraoral scanner within ten minutes of completion. Then, the edges of the individual tray for ZOE will be shaped with impression compound to ensure peripheral closure. The impression will be completed with zinc-oxide eugenol impression material. The impression will be digitized. These measurements will then be compared using a reverse-engineering program (Geomagic design X version 2016.1.0, 3D Systems Inc. Rock Hill, SC). Before the comparison, in the same program, the parts to be evaluated on the ZOE in the conventional group and A.I OFF in the digital group will be divided into regions. These areas will be divided into four sections as right and left vestibular region, postdam area, hard palate region, except for the A.I OFF-MOD comparison group. In the A.I OFF-MOD comparison group, it will include the right and left initial areas, including the areas where scanning starts in the second scan of the MOD method. In addition, all measurements will be compared in terms of the whole surface and all measurement boundaries including the whole measurement surface as one. The comparison groups are ZOE-ALG, ZOE-A.I OFF, A.I OFF-A.I ON, A.I OFF-MOD. The measurements in the comparison groups will be overlapped first with the initial alignment and then with the best fit alignment algorithm. All sections will be evaluated individually with the "3D compare" feature and the amount of deviation in the areas to be evaluated will be determined.

02

Conditions studied

  • Edentulous Jaw

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Keywords

  • Edentulous Jaw
  • Digital Impression
  • Physical Impression
03

In context

Jaw, Edentulous

175 studies on the registry are indexed under Jaw, Edentulous; 24 are open to participants now.

This study's enrollment of 15 is below the median of 31 across 148 interventional studies indexed under Jaw, Edentulous.

Browse Jaw, Edentulous studies →

Lead sponsor

Hacettepe University is the lead sponsor of 1,001 studies on the registry; 215 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Volunteers who had been using maxillary complete denture for at least 3 months
  • Volunteers were clinically evaluated for healthy oral mucosa

Exclusion criteria

Exclusion Criteria:

  • Volunteers who had general health problems
  • Volunteers who had of tissue hyperplasia, labile alveolar crest, allergic reaction to the prosthesis, percussion or mucosal irritation
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
15 participants (actual)

Study arms

  • Other
    Irreversible Hydrocolloid

    Final impression taken with irreversible hydrocolloid impression material and stock tray in single step.

    Other: Edentulous maxilla final impression for complete denture

  • Other
    Zinc Oxide Eugenol

    Final impression taken with zinc oxide eugenol impression material and individual tray in two steps.

    Other: Edentulous maxilla final impression for complete denture

  • Other
    Intraoral Scanner - Artificial Intelligence Off

    Final impression taken with intraoral scanner in artificial intelligence mode deactivated in single step.

    Other: Edentulous maxilla final impression for complete denture

  • Other
    Intraoral Scanner - Artificial Intelligence On

    Final impression taken with intraoral scanner in artificial intelligence mode activated in single step.

    Other: Edentulous maxilla final impression for complete denture

  • Other
    Intraoral Scanner - Modified

    Final impression taken with intraoral scanner in two steps using occlusal rim.

    Other: Edentulous maxilla final impression for complete denture

Interventions

  • OtherEdentulous maxilla final impression for complete denture

    Final impressions of edentulous maxilla separated in two groups. In physical impression group stock and individual trays and physical impression materials used.

06

What researchers measure

Primary outcomes

  1. Three Dimensional Difference Between Irreversible Hydrocolloid and Zinc Oxide Eugenol Impressions

    Evaluation of the three-dimensional difference between two impressions using a reverse-engineering program and quantification of the deviation

    Time frame: Through study completion, an average of 6 months

  2. Three Dimensional Difference Between Zinc Oxide Eugenol and Intraoral Scanner AI Off Impressions

    Evaluation of the three-dimensional difference between two impressions using a reverse-engineering program and quantification of the deviation

    Time frame: Through study completion, an average of 6 months

  3. Three Dimensional Difference Between Intraoral Scanner AI Off and AI On Impressions

    Evaluation of the three-dimensional difference between two impressions using a reverse-engineering program and quantification of the deviation

    Time frame: Through study completion, an average of 6 months

  4. Three Dimensional Difference Between Intraoral Scanner AI Off and Modified Impressions

    Evaluation of the three-dimensional difference between two impressions using a reverse-engineering program and quantification of the deviation

    Time frame: Through study completion, an average of 6 months

07

Study locations

1 site
  • Hacettepe University Faculty of Dentistry
    Ankara, Altındağ, Turkey (Türkiye)
08

References and documents

Publications

  • Lo Russo L, Salamini A, Troiano G, Guida L. Digital dentures: A protocol based on intraoral scans. J Prosthet Dent. 2021 Apr;125(4):597-602. doi: 10.1016/j.prosdent.2020.02.006. Epub 2020 Apr 21. PubMed 32331785 ↗
  • Lo Russo L, Caradonna G, Troiano G, Salamini A, Guida L, Ciavarella D. Three-dimensional differences between intraoral scans and conventional impressions of edentulous jaws: A clinical study. J Prosthet Dent. 2020 Feb;123(2):264-268. doi: 10.1016/j.prosdent.2019.04.004. Epub 2019 May 29. PubMed 31153614 ↗
  • Chebib N, Kalberer N, Srinivasan M, Maniewicz S, Perneger T, Muller F. Edentulous jaw impression techniques: An in vivo comparison of trueness. J Prosthet Dent. 2019 Apr;121(4):623-630. doi: 10.1016/j.prosdent.2018.08.016. Epub 2018 Dec 21. PubMed 30580982 ↗
  • Kahya Karaca S, Akca K. Comparison of conventional and digital impression approaches for edentulous maxilla: clinical study. BMC Oral Health. 2024 Nov 14;24(1):1378. doi: 10.1186/s12903-024-05151-3. PubMed 39543593 ↗

Study documents

  • Protocol and statistical analysis plan · May 9, 2022
  • Informed consent form · May 9, 2022

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jul 2022 to primary completion in Dec 2023, 17 months.

Of 71 non-industry interventional studies with no phase under Jaw, Edentulous, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 34. This study's 17 months is close to that.

Counting every sponsor, half of 87 studies reached it within 25 months; a quarter within 13 and three quarters within 51.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 29, 2024
First posted
May 6, 2024
StartActual
Jul 30, 2022
Primary completionActual
Dec 30, 2023
CompletionActual
Mar 27, 2024
Last update
May 6, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 6, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06400277
Responsible party
Sinem Kahya Karaca (Research Assistant, Hacettepe University) — Principal investigator
First posted
May 6, 2024
Start date
Jul 30, 2022
Primary completion
Dec 30, 2023
Completion
Mar 27, 2024
Last update
May 6, 2024

Study contacts

Sinem Kahya Karaca
principal investigator · Hacettepe University
Kıvanç Akça, Prof. Dr.
study director · Hacettepe University

Oversight

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

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