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CompletedNCT07266844Updated Dec 5, 2025

CAPSULaser in Cases of Intumescent Cataract

An interventional study of CAPSULaser and capsulotomy in Intumescent Cataract, sponsored by Zagazig University. Completed at 1 site in Saudi Arabia. Per ClinicalTrials.gov, last updated 2025-12-05.

Sponsored by Zagazig University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Jul 2025, registered Nov 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Not applicable
Sex
All
01

Study summary

evaluating the use of selective laser in doing capsulotomy in intumescent cataract

Read the detailed description

Evaluating the safety and advantages of using selective laser capsulotomy for capsulorhexis creation in intumescent cataract

02

Conditions studied

  • Intumescent Cataract

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Keywords

  • cataract
03

In context

Cataract

1,701 studies on the registry are indexed under Cataract; 230 are open to participants now.

This study's enrollment of 24 is below the median of 80 across 1,155 interventional studies indexed under Cataract.

Browse Cataract studies →

Lead sponsor

Zagazig University is the lead sponsor of 447 studies on the registry; 75 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • patients with intumescent cataract and good pupil dilatation

Exclusion criteria

Exclusion Criteria:

  • absence of corneal scaring
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Other
    intumescent cataract

    CAPSULaser

    Procedure: CAPSULaser · Device: capsulotomy

Interventions

  • ProcedureCAPSULaser

    doing capsulotomy using CAPSULaser

  • Devicecapsulotomy

    capsulorhexis using CAPSULaser

06

What researchers measure

Primary outcomes

  1. To measure the actual size compared to result size as measured by slit lamp in mm

    To measure the actual size compared to result size as measured by slit lamp

    Time frame: 3 months

  2. Incidence and number of extended capsulorhexis to the total number of cases

    Incidence and number of extended capsulorhexis

    Time frame: 1 month

07

Study locations

1 site
  • Magrabi eye hospitals
    Jeddah, Jedda 22233, Saudi Arabia
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 5, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07266844
Lead sponsor
Zagazig University
Responsible party
Sponsor
First posted
Dec 5, 2025
Start date
Jul 8, 2025
Primary completion
Nov 6, 2025
Completion
Nov 6, 2025
Last update
Dec 5, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2025. You cannot join it, but the record below documents what was studied.

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