Last reviewed · How we verify
NCT05943912
Myopia Control Effect of DIMS Spectacle Lenses in Czech Children and Young Adults
trial testing Single Vision Spectacle Lens in Myopia in 80 participants. Participants enrolled and being followed up; not accepting new ones.
10 October 2026
Quick facts
| Lead sponsor | Czech Technical University in Prague |
|---|---|
| Status | Active, enrolled |
| Study type | OBSERVATIONAL |
| Enrollment | 80 |
| Start date | 17 April 2023 |
| Primary completion | 10 October 2026 |
| Estimated completion | 12 December 2026 |
| Sites | 1 location across Czechia |
Drugs / interventions tested
- Single Vision Spectacle Lens
- Defocus Incorporated Multiple Segments (DIMS) Spectacle Lens
Conditions studied
- Myopia — all drugs for Myopia →
Sponsor
Czech Technical University in Prague
Who can join
Adults 6 to 26, any sex, with Myopia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The aim of this clinical study is to compare the efficacy of DIMS technology spectacle lenses with conventional single vision spectacle lenses at slowing the progression of myopia in the category of children and young adults during three years.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Efficacy of Spectacle Correction Using Defocus Incorporated Multiple Segments in the Myopic Population.
Zakova M, Fus M, Tejkl L. · · 2025 · PMID 40927114 · DOI 10.2147/opth.s541232
Verify or expand the search:
- PubMed search for NCT05943912
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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Other Czech Technical University in Prague trials
Trials by the same sponsor.
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- NCT06635018 — Effect of Pulse Oximeter Device on Measured Perfusion Index Values · NA · completed
- NCT06098092 — Long-term Accuracy and Stability of Blood Pressure Measurements From a Smartwatch: Prospective Validation Study · NA · completed
- NCT05929196 — Feasibility Evaluation - Blood Glucose Level Monitoring by Microwave Metamaterial Sensor in Blood Samples. · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05943912 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Czech Technical University in Prague
- Last refreshed: 2 April 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05943912.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing