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A study on experiences of patients undergoing injection in back part of their eye.

A prospective study of patient experiences at different stages of the intravitreal anti vascular endothelial growth factor injection.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/01/016907
Enrollment
174
Registered
2019-01-04
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: H350- Background retinopathy and retinalvascular changes

Interventions

None listed

Sponsors

Aravind Eye Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with visual acuity better than 6/60 undergoing intravitreal anti VEGF [vascular endothelial growth factor] for following pathologies. 2.Retinal Venous Occlusion Diseases [RVOD]. 3.Diabetic Macular Edema [DME]. 4.Age related Macular Degeneration [AMD]. 5.Polypoidal Choroidal Vasculopathy [PCV].

Exclusion criteria

Exclusion criteria: 1.Patients planned for vitrectomy after anti VEGF[vascular endothelial growth factor]. 2.Neo Vascular Glaucoma [NVG]. 3.Uncontrolled hypertension (>= 160 mm Hg systolic or >= 100 mm Hg diastolic), with or without anti-hypertensive medications. 4.Patients consuming drugs that influence cardiac rate and rhythm (like Beta-blockers). 5.Uncontrolled Diabetes Mellitus (FBS >= 180 mg/dl), despite medications. 6.Patients with dementia, hearing impairment, speech disorder, mental retardation, or patients with any psychiatric ailments, or on any psychiatric medications. 7.Patients with Uveitis. 8.Patients with ocular manifestations of diabetes other than retinopathy-Diabetic neuropathy.

Design outcomes

Primary

MeasureTime frame
1) To quantitatively describe the patientsâ?? experiences by determining their opinion [distress level] on the whole injection processTimepoint: 1 year from starting day of study.

Secondary

MeasureTime frame
2) To assess subjectively (by means of questionnaire) and objectively(by measuring vital signs- pre injection, during injection, post injection) visual experience of patients undergoing intravitreal anti vascular endothelial growth factor.Timepoint: 1 year from starting day of study.

Countries

India

Contacts

Public ContactDr Suresh Mekala

Aravind Eye Hospital

pankajadhoble@yahoo.co.in0413-2619100

Outcome results

None listed

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