WHO ICTRP trial
A Postmarketing Clinical follow up observational study to evaluate safety and…
CTRI/2021/10/037105 · Clinical Trials Registry India (CTRI) · Recruiting
Key facts
| Trial ID | CTRI/2021/10/037105 |
|---|---|
| Public title | A Postmarketing Clinical follow up observational study to evaluate safety and effectiveness of hydrophilic acrylic (intraocular) lens.CT ASPHINA 509 M/MP |
| Scientific title | Retro-prospective evaluation of the clinical safety and effectiveness of hydro- philic acrylic intraocular lens - UVEA 509 |
| Primary sponsor | Carl Zeiss Meditec AG |
| Registry | Clinical Trials Registry India (CTRI) |
| Recruitment status | Recruiting |
| Study type | PMS |
| Phase | Post Marketing Surveillance |
| Countries | India;France;Spain |
| Conditions | Health Condition 1: H270- Aphakia |
| Interventions | Intervention1: CT ASPHINA 509M/MP: The intraocular lens CT ASPHINA 509M/MP is intended for implantation in the capsular bag to replace the human crystalline lens Intervention2: ASPHINA 509 BER-401-20 : Mfg By: Carl Zeiss Meditec AG… |
| Registration date | May 10, 2021 |
| Target size | 325 |
| Secondary IDs | ASPHINA 509 BER-401-20 Version v3 dated 30.06.2021 |
| Registry page | ctri.nic.in |
At a glance
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About WHO ICTRP trial registrations
The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.
Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: