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Study on the Use of Micropulse Laser to Treat Central Serous Chorioretinopathy

A Prospective Study of the Use of Micropulse 577nm Laser Treatment in Central Serous Chorioretinopathy

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01982383
Enrollment
2
Registered
2013-11-13
Start date
2012-11-30
Completion date
2015-11-30
Last updated
2018-03-27

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

Conditions

Central Serous Chorioretinopathy

Keywords

CSC, Edema, Retinopathy

Brief summary

The investigators hypothesis is that using the micropulse laser in patient with Central Serous Chorioretinopathy (CSC) will prompt resolution of CSC and will be effective in significantly minimizing visual recovery time from this disease as well as potentially preventing recurrences.

Detailed description

The investigators hypothesize that application of 577nm micropulse laser in patients with CSC will prompt resolution of CSC as measured by ocular coherence tomography and best corrected visual acuity. This will be a pilot study to establish sound methods and provide some insights to the safety and efficacy of CSC treatment.

Interventions

OTHERNo treatment

Sponsors

George Washington University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Patients with new diagnosis of CSC and no other comorbidities or prior retinal treatment * Patients ranging from 30 to 60 years of age

Exclusion criteria

* Patients with no case of CSC * Patients with other macular comorbidities including but not limited to diabetic retinopathy, macular degeneration * Patients with prior retinal treatment

Design outcomes

Primary

MeasureTime frameDescription
Resolution of Fluid Build-upwithin 1 week to 3 months after the laser procedure is completedCentral Serous Choroidopathy is a disease that causes fluid to build up under the retina,the back part of the inner eye that sends sight information to the brain. The objective here is to apply 577nm of micropulse laser to see if CSC resolution occurs and measuring it through ocular coherence tomography (retinal imaging), vision score, and visual field testing for retinal sensitivity.

Countries

United States

Participant flow

Participants by arm

ArmCount
Micropulse Laser Treatment
Patient's randomized to ML treatment would be treated with the following settings: 200 micron spot size, 0.2 second duration, 15% duty cycle, and 300 milliWatt power. Their eyes would be dilated prior to treatment with standard mydriatic medications, including Tropicamide and Phenylephrine Micropulse Laser Treatment
2
No Treatment
Patients randomized to this treatment arm, will not receive treatment for CSC. They will continue to be observed at month 1 and month 3. If any worsening of pathology is found during the follow up visits, the patient will be removed from the study and given appropriate standard of care by the attending No treatment
0
Total2

Baseline characteristics

CharacteristicMicropulse Laser TreatmentTotal
Age, Categorical
<=18 years
0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
2 Participants2 Participants
Sex: Female, Male
Female
2 Participants2 Participants
Sex: Female, Male
Male
0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 20 / 0
other
Total, other adverse events
0 / 20 / 0
serious
Total, serious adverse events
0 / 20 / 0

Outcome results

Primary

Resolution of Fluid Build-up

Central Serous Choroidopathy is a disease that causes fluid to build up under the retina,the back part of the inner eye that sends sight information to the brain. The objective here is to apply 577nm of micropulse laser to see if CSC resolution occurs and measuring it through ocular coherence tomography (retinal imaging), vision score, and visual field testing for retinal sensitivity.

Time frame: within 1 week to 3 months after the laser procedure is completed

Population: No data analyzed. Study terminated due to lack of enrollment

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026