Clinical trial for visual function and safety evaluation:Artificial posterior capsule construction surgery and Intraocular lens implantation with 10-0 Polypropylene surgical suture which have been used for Scleral suture fixation of intraocular lenses

Clinical trial for visual function and safety evaluation:Artificial posterior capsule construction surgery and Intraocular lens implantation with 10-0 Polypropylene surgical suture which have been used for Scleral suture fixation of intraocular lenses - Clinical trial for visual function and safety evaluation:Artificial posterior capsule construction surgery and Intraocular lens implantation

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000015145

Enrollment

Registered

2015-04-01

Start date

2014-09-12

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

aphakia

Interventions

Artificial posterior capsule construction surgery and Intraocular lens implantation

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) patiants with aphakia 2) not less than age of 20 3) male and female 4) patiants who take informed consent

Exclusion criteria

Exclusion criteria: 1) patiants who is inappropriate for this trial

Design outcomes

Primary

Measure	Time frame
safety	—

Secondary

Measure	Time frame
efficacy of visual fanction,freqency of intraoperative and postoperative complications	—

Countries

Japan

Contacts

Public ContactMmichio Matsunaga

Yamaguchi university hospital ophthalmology

michio_nchu214@yahoo.co.jp0836222278

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026