Last reviewed · How we verify
NCT05646004
621 Real World Study
NA trial testing Cataract surgery in Senile Cataract in 105 participants. Status unknown.
1 September 2024
Quick facts
| Lead sponsor | Carl Zeiss Meditec AG |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 105 |
| Start date | 9 January 2023 |
| Primary completion | 1 September 2024 |
| Estimated completion | 1 September 2024 |
| Sites | 1 location across China |
Drugs / interventions tested
- Cataract surgery — full drug profile →
Conditions studied
- Senile Cataract — all drugs for Senile Cataract →
Sponsor
Carl Zeiss Meditec AG — full company profile →
Who can join
18 and older, any sex, with Senile Cataract. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study is evaluating the clinical safety and effectiveness of 621, after cataract surgery.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05646004
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Cataract surgery
Trials testing the same drug.
- NCT06505434 — A Dynamic Study of Pupil Diameter After Artificial Lens Implantation in Patients With High Myopia · not yet recruiting
- NCT06400745 — Clareon PanOptix Pro vs. Clareon PanOptix - Study A · NA · completed
- NCT05776095 — Evaluation of Safety and Performance Outcomes of Eyedeal IOL Implantation After Cataract Removal · NA · unknown
- NCT05796674 — Clareon IOL Retrospective Data Collection · completed
- NCT04074954 — A (Prospective/Pilot) Study Evaluating the Effect of Cataract Surgery on the Daily Activity Levels of Elderly Patients · withdrawn
Other Carl Zeiss Meditec AG trials
Trials by the same sponsor.
- NCT07471295 — Toric Performance And Constant Evaluation · Phase 4 · not yet recruiting
- NCT07297719 — Evaluation of Glistening, Visual Outcomes and General Safety 24 Months Post-IOL Implantation · completed
- NCT06192901 — Safety and Performance of Hydrophobic and Hydrophilic Intraocular Lenses After Bilateral Cataract Surgery · completed
- NCT06247683 — Study to Confirm Safety and Performance of a New Multifocal IOL · NA · completed
- NCT05201027 — Study to Optimize the IOL Constant of a New Multifocal Intraocular Lens · NA · terminated
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 NCT05646004 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Carl Zeiss Meditec AG
- Last refreshed: 10 January 2023
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/NCT05646004.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing