Subthreshold Micropulse Laser Treatment of Acute Central Serous Chorioretinopathy

Sponsor
Minia University (Other)
Overall Status
Completed
CT.gov ID
NCT05447117
Collaborator
(none)
42
1
32.5
1.3

Study Details

Study Description

Brief Summary

To evaluate the efficacy and safety of 532 nm green subthreshold micropulse laser (GSML) as a treatment for acute central serous chorioretinopathy (CSCR).

Condition or Disease Intervention/Treatment Phase
  • Procedure: Micropulse laser
N/A

Detailed Description

This prospective study included 42 eyes of 42 patients with acute CSCR treated with IRIDEX™ IQ 532 nm GSML. The study was conducted at Minia University Hospital and Genaidy Ophthalmology Center, Minia, Egypt between October 2019 and May 2022. All patients were subjected to a complete ophthalmological examination, fluorescein angiography (FA) and optical coherence tomography (OCT) at baseline and each follow-up visit 1, 3 and 18 months after laser treatment

Study Design

Study Type:
Interventional
Actual Enrollment :
42 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Subthreshold Micropulse 532 nm Green Laser Treatment of Acute Central Serous Chorioretinopathy: 18-month Results
Actual Study Start Date :
Oct 15, 2019
Actual Primary Completion Date :
May 30, 2022
Actual Study Completion Date :
Jun 30, 2022

Outcome Measures

Primary Outcome Measures

  1. change in visual acuity [18 months]

    resolution of subretinal fluid

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • acute CSCR
Exclusion Criteria:
  • chronic CSCR Previously treated case of Acute CSCR

Contacts and Locations

Locations

Site City State Country Postal Code
1 Minia University Hospital Minya Minia Egypt 61111

Sponsors and Collaborators

  • Minia University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hosny Ahmed Zein, DR, Minia University
ClinicalTrials.gov Identifier:
NCT05447117
Other Study ID Numbers:
  • CSCR2019
First Posted:
Jul 7, 2022
Last Update Posted:
Jul 7, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 7, 2022