Study of visual gain after secondary IOL implantation in aphakic eyes

Evaluation of visual outcome of secondary intraocular lens implantation for managing patients with aphakia in developing countries: A prospective interventional study

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/10/058327

Enrollment

Registered

2023-10-05

Start date

Unknown

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

Health Condition 1: H270- Aphakia

Interventions

Intervention1: Intraocular lens implantation: A single group of 50 Aphakic eyes will be our series. Based on slitlamp examination site of implnataion of IOL will be decided and thereafter biometry wil

Eligibility

Inclusion criteria

Inclusion criteria: Bilateral Aphakia Aphakia with fellow eye pseudophakic or having crystaline lens All Traumatic Aphakia irrespective of corneoscleral tear

Exclusion criteria

Exclusion criteria: Advanced OSD Glaucoma being treated or trabeculectomy done in that eye Decompensated cornea or liklihood of decompensation in future

Design outcomes

Primary

Measure	Time frame
To observe the best corrected visual acuity after secondary IOL implantation individually for each eye at the end of 12 weeks from date of intraocular lens implantation.Timepoint: 12 weeks after implantation.	—

Secondary

Measure	Time frame
Intra and post op complications will be noted. Safety of secondary IOL will be analysed Timepoint: 21 months	—

Countries

India

Contacts

Public ContactDr Lubna Khan

AIIMS RAIPUR

lubnakhan65@yahoo.co.in7869913118

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026