ClinicalTrials.gg
CompletedNCT07926035Updated Nov 9, 2026

Intraoral Aging of 3D Printed Orthodontic Aligners

An interventional study of TC-85 directly 3D-printed aligner and TA-28 directly 3D-printed aligner in Orthodontic Aligners, sponsored by Alexandria University. Completed at 1 site in Egypt. Open to participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2026-11-09.

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

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Feb 2026, registered Oct 2026).
Updated Nov 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

This study aims to bridge the gap in literature by conducting a combined evaluation of the mechanical, chemical, optical, and morphological changes of 3D-printed clear aligners manufactured from TC-85 and TA-28 resins that occur after clinical use. By analyzing aligners retrieved after two weeks of intraoral use, this research will offer critical insights into the material stability and aging behavior of the two types of 3D-printed clear aligners.

Read the detailed description

Background: Direct 3D-printing of clear aligners is emerging as a promising alternative to conventional thermoformed systems, offering enhanced precision, digital workflow efficiency, and improved material control. Among the photopolymer resins used for 3D-printed aligners, Tera Harz TC-85 and Tera Harz TA-28 have emerged as leading materials due to their reported shape-memory behavior, dimensional stability, and mechanical performance. However, despite increasing clinical adoption, limited evidence exists regarding how these two materials respond to intraoral aging, where fluctuating pH, temperature changes, salivary enzymes, and occlusal forces may alter their mechanical, optical, chemical, and surface characteristics. Understanding these changes is essential for determining the clinical reliability and long-term performance of each resin.Therefore, a demanding evaluation of post-aging changes in 3D-printed aligners is essential to determine their suitability for sustained orthodontic force delivery and to guide material selection in clinical practice. Assessing how key properties such as mechanical behavior, dimensional accuracy, surface topography, and optical characteristics evolve after intraoral exposure will provide valuable insight into material durability and clinical reliability.

02

Conditions studied

  • Orthodontic Aligners

Keywords

  • Orthodontic aligners; Printing, three-dimensional; Degree of conversion; Elastic modulus; Hardness; Intraoral aging; Polymerization
03

In context

Lead sponsor

Alexandria University is the lead sponsor of 604 studies on the registry; 140 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  • Patients aged 18-35 years.
  • Mild to moderate crowding.
  • Good oral hygiene and healthy periodontium.
  • Permanent dentition with no active caries.

Exclusion criteria

Exclusion Criteria:

  • Patients with systemic diseases affecting saliva or oral mucosa.
  • Smoking or alcohol consumption.
  • History of parafunctional habits.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
12 participants (actual)

Study arms

  • Experimental
    TC-85 maxillary / TA-28 mandibular

    Participants received a directly 3D-printed TC-85 aligner in the maxillary arch and a directly 3D-printed TA-28 aligner in the mandibular arch. Both aligners were worn simultaneously for 2 weeks (22 hours/day).

    Device: TC-85 directly 3D-printed aligner

  • Experimental
    TA-28 maxillary / TC-85 mandibular

    Participants received a directly 3D-printed TA-28 aligner in the maxillary arch and a directly 3D-printed TC-85 aligner in the mandibular arch. Both aligners were worn simultaneously for 2 weeks (22 hours/day).

    Device: TA-28 directly 3D-printed aligner

Interventions

  • DeviceTC-85 directly 3D-printed aligner

    Aligner directly 3D-printed from Tera Harz TC-85 shape-memory resin \[add printer, layer thickness and post-curing protocol\]. Worn 22 hours/day for 2 weeks in the maxillary or mandibular arch, according to a computer-generated randomization sequence.

  • DeviceTA-28 directly 3D-printed aligner

    Aligner directly 3D-printed from Tera Harz TA-28 shape-memory resin \[same printer, layer thickness and post-curing protocol as above\]. Worn 22 hours/day for 2 weeks in the maxillary or mandibular arch, according to a computer-generated randomization sequence.

06

What researchers measure

Primary outcomes

  1. Change in indentation hardness (HIT), measured by instrumented nanoindentation

    Indentation hardness (HIT, GPa) of directly 3D-printed TC-85 and TA-28 aligners, measured by instrumented nanoindentation using a Nano Indenter XP (MTS Systems Corporation, USA) with a Berkovich diamond indenter. Tests were displacement-controlled to a maximum depth of 2000 nm at a constant strain rate of 0.05 s-¹, with 25 indentations per specimen spaced 30 μm apart. Testing followed ISO 14577-1:2015 and data were analyzed by the Oliver and Pharr method. Retrieved aligners are compared with unused aligners printed from the same digital design.

    Time frame: Baseline (unused aligner) and after 2 weeks of intraoral use

Secondary outcomes

  1. Change in indentation elastic modulus (EIT), measured by instrumented nanoindentation

    Indentation elastic modulus (EIT, GPa) of directly 3D-printed TC-85 and TA-28 aligners, measured by instrumented nanoindentation using a Nano Indenter XP (MTS Systems Corporation, USA) with a Berkovich diamond indenter. Tests were displacement-controlled to a maximum depth of 2000 nm at a constant strain rate of 0.05 s-¹, with 25 indentations per specimen spaced 30 μm apart. A Poisson's ratio of 0.4 was assumed. Testing followed ISO 14577-1:2015 and data were analyzed by the Oliver and Pharr method. Retrieved aligners are compared with unused aligners printed from the same digital design.

    Time frame: Baseline (unused aligner) and after 2 weeks of intraoral use

  2. Change in color (ΔE₀₀, CIEDE2000), measured by UV-visible spectrophotometry

    Color of directly 3D-printed TC-85 and TA-28 aligners measured with a UV-visible spectrophotometer (V-770, JASCO Corporation, Tokyo, Japan). Each aligner was sectioned along the right central incisor-canine region, and the labial surface was positioned in a standardized manner facing the incident-light window. CIE Lab\* coordinates were recorded according to ISO 11664-4:2019, and the color change between unused and retrieved aligners was calculated as ΔE₀₀ using the CIEDE2000 equation (parametric factors set to 1). Values are interpreted against 0.8 (50:50% perceptibility) and 1.8 (50:50% acceptability).

    Time frame: Baseline (unused aligner) and after 2 weeks of intraoral use

  3. Change in light transmittance and absorbance (400-700 nm), measured by UV-visible spectrophotometry

    Light transmittance and absorbance of TC-85 and TA-28 aligners recorded across the visible range (400-700 nm) with a UV-visible spectrophotometer (V-770, JASCO Corporation, Tokyo, Japan) using Spectra Manager II software, after calibration according to the manufacturer's instructions. Values at 400 and 700 nm were extracted from each spectrum and compared between materials and between unused and retrieved aligners.

    Time frame: Baseline (unused aligner) and after 2 weeks of intraoral use

  4. Change in aligner thickness (μm), measured by confocal laser scanning microscopy

    Thickness of TC-85 and TA-28 aligners measured by confocal laser scanning microscopy (Leica DMi8, Leica Microsystems, Wetzlar, Germany) with a 10× objective and 1.5× digital zoom under standardized imaging conditions. Standardized 4 × 4 mm specimens were taken from the labial surface of the left central incisor region. Z-stack images were reconstructed in 3D using Leica LAS AF software (version 1.1.0.12420), and thickness was calculated as the perpendicular distance between the upper and lower specimen surfaces. Each specimen was measured twice and the mean was used.

    Time frame: Baseline (unused aligner) and after 2 weeks of intraoral use

  5. Change in surface roughness (Sa, Sq, Sp, Sv), measured by confocal laser scanning microscopy

    Surface roughness of the inner surface of directly 3D-printed TC-85 and TA-28 aligners, assessed on the same 4 × 4 mm specimens used for thickness measurement, imaged by confocal laser scanning microscopy (Leica DMi8, Leica Microsystems, Wetzlar, Germany). Height maps generated from the z-stacks with Leica LAS AF software were analyzed in ImageJ (National Institutes of Health, USA) with the SurfCharJ-1q plugin to calculate Sa (arithmetical mean height), Sq (root mean square height), Sp (maximum peak height) and Sv (maximum valley depth), in µm. Analysis was repeated twice per specimen and the mean was used. Identical acquisition and analysis settings were applied to all specimens.

    Time frame: Baseline (unused aligner) and after 2 weeks of intraoral use

  6. Change in degree of conversion (DC), measured by ATR-FTIR spectroscopy

    Degree of conversion (%) of TC-85 and TA-28 aligners, calculated from attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectra as the reduction of the aliphatic C=C band near 1638 cm-¹ relative to, referenced to the corresponding unset resin. Retrieved aligners are compared with unused aligners.

    Time frame: Baseline (unused aligner) and after 2 weeks of intraoral use

  7. Change in chemical structure, assessed by ATR-FTIR spectral analysis

    Qualitative comparison of ATR-FTIR spectra of unused and retrieved TC-85 and TA-28 aligners, focusing on the O-H/N-H stretching bands (3400-3200 cm-¹), aliphatic C-H bands (about 2920 and 2850 cm-¹), the carbonyl (C=O) band (about 1700 cm-¹) and the C-O/C-O-C region (1200-1000 cm-¹).

    Time frame: Baseline (unused aligner) and after 2 weeks of intraoral use

07

Study locations

1 site
  • Department of Orthodontics, Faculty of Dentistry, Alexandria University
    Alexandria, Alexandria Governorate 21526, Egypt
08

References and documents

Individual participant data

Plan to share: Undecided — Individual participant data will not be shared publicly because of participant confidentiality and privacy considerations. The study involves a relatively small sample, and sharing individual-level data may pose a risk of participant identification. De-identified aggregate results will be reported in the published manuscripts. Data may be made available from the corresponding author upon reasonable request, subject to institutional ethical approval and applicable data-protection requirements.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Feb 2026 to primary completion in Apr 2026, 2 months.

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

Registered
Oct 31, 2026
First posted
Nov 9, 2026
StartActual
Feb 1, 2026
Primary completionActual
Apr 1, 2026
CompletionActual
Sep 1, 2026
Last update
Nov 9, 2026
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.
Registered
First appeared on the registry. No changes since
Nov 9, 2026
Show all 1 update
  1. Nov 9, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07926035
Responsible party
Azza Gamal Kamel Wafa (Assistant Lecturer, University of Alexandria) — Principal investigator
First posted
Nov 9, 2026
Start date
Feb 1, 2026
Primary completion
Apr 1, 2026
Completion
Sep 1, 2026
Last update
Nov 9, 2026

Study contacts

Azza Gamal Wafa, PHD
principal investigator · Alexandria University

Oversight

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

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