NIPH Clinical Trials Search

JRCT ID: jRCT2032210035

Registered date:12/04/2021


Basic Information

Recruitment status Not Recruiting
Health condition(s) or Problem(s) studiedCataract
Date of first enrollment02/07/2021
Target sample size100
Countries of recruitment
Study typeInterventional
Intervention(s)Implantation of intraocular after cataract surgery


Primary OutcomeVisual acuity after lens implantation. Incidence of adverse events and defects.
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum>= 20age old
Age maximumNot applicable
Include criteriaPatients who scheduled to remove the crystalline lens by phacoemulsification and aspiration
Exclude criteriaPatients with indication for secondary lens implantation. Patients with uncontrolled glaucoma. Pregnant women, lactating women or women who desire to be pregnant. Patients who are judged inappropriate to participate in the study by principal investigator or sub-investigator.

Related Information


Public contact
Name Hideyuki Kami-ie
Address 2-2, Nihonbashi Honcho 2-chome, Chuo-ku Tokyo Tokyo Japan 103-8830
Telephone +81-3-3279-0370
Affiliation Wakamoto Pharmaceutical Co., Ltd.
Scientific contact
Name Kazuo Ichikawa
Address 12-22, Sanbonmatsu-cho Atuta-ku, Nagoya-shi, Aichi-ken Aichi Japan 456-0032
Telephone +81-52-883-1543
Affiliation Chukyo Eye Clinic