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A study to assess how certain eye scan markers in a condition called Idiopathic Epiretinal Membrane relate to the patients Vision.

A Retrospective study to find the association between OCT biomarkers of Idiopathic Epiretinal Membrane and Visual Acuity - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/12/077637
Enrollment
84
Registered
2024-12-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: H35- Other retinal disorders

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Department of Ophtalmology Kasturba Medical College Manipal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Presence of Unilateral or Bilateral Epiretinal Membrane whose aetiology cannot be traced back to any disease.

Exclusion criteria

Exclusion criteria: 1.Epiretinal membrane secondary to any previous ocular surgery, any trauma to the eye, any systemic co-morbidity like Diabetes mellitus leading to Proliferative and Non-proliferative diabetic retinopathy. 2.Any ocular infection or any non -infectious inflammatory condition of the eye. 3.History of Retinal Detachment (traumatic/exudative/rhegmatogenous) 4.Known case of Advanced Glaucoma or Optic Neuropathy 5.Patients diagnosed with any other cause of vision loss other than Epiretinal Membrane

Design outcomes

Primary

MeasureTime frame
This study aims to bring forth the often ignored parameters that are seen on OCT in patients with Idiopathic Epiretinal membrane and this understanding will help guide the treatment plan of the patients in the future by means of acting as a more reliable indicator of the patient’s visual prognosis. It will also help ascertain the urgency of surgical intervention in the patientTimepoint: Assessment of the data of the patient at their first visit, followed by assessment at 3 to 6 months time interval from the first visit

Secondary

MeasureTime frame
Analysis of subjects with two sequential OCTs done with a time interval of 3 to 6 months between them, to assess the longitudinal changes in the OCT biomarkers & to determine which Biomarker is associated with worse Visual Acuity.Timepoint: Assessment of the data of the patient at their first visit, followed by assessment at 3 to 6 months time interval from the first visit

Countries

India

Contacts

Public ContactDr Tanya Sharma

Kasturba Medical College, Manipal

bhatshenoys@gmail.com9686125861

Outcome results

None listed

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