Effectiveness of Prism Spectacles in Patients With Age Related Macular Degeneration

NCT ID: NCT05437302

Last Updated: 2022-06-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-10-04

Study Completion Date

2022-05-31

Brief Summary

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A study is conducted to determine the effectiveness of prism spectacles in improving visual acuity with age related macular degeneration patients and to assess the improvement in quality of life in patients by using prism spectacles.

Detailed Description

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A random sampling technique will be used to allocate patient in interventional and non-interventional group. The diagnosed patients of age-related macular degeneration are assessed for prism spectacles for near vision and prism glasses will be dispensed to the patients. Each subject will be interviewed to fill the Proforma after taking the informed consent. The results of this study will show the effectiveness of prism glasses in patients with age related macular degeneration in their daily routine near work as compared to conventional glasses.

Conditions

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Age-Related Macular Degeneration

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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interventional

prism spectacles prescribed

Group Type EXPERIMENTAL

prism spectacle

Intervention Type DEVICE

a prism is dispensed in prescription glasses

non interventional

presbyopia glasses prescribed

Group Type ACTIVE_COMPARATOR

prism spectacle

Intervention Type DEVICE

a prism is dispensed in prescription glasses

Interventions

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prism spectacle

a prism is dispensed in prescription glasses

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients having age \>50 years with age related macular degeneration.
* Patients of both genders (male and female).
* Participants who will be willing to give informed consent for participation in the study.

Exclusion Criteria

* Presence of all ocular disease and systemic ocular pathologies able to impair visual function.
* Presence of disorders causing choroidal neovascularization other than age related macular degeneration.
* Patients with mental illness, dementia, and severe physical limitations
Minimum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Faisalabad

OTHER

Sponsor Role lead

Responsible Party

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mehreen tanveer

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ayesha Kiran

Role: STUDY_DIRECTOR

University of Faisalabad

Locations

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Mehreen

Rawalpindi, , Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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Ufaisalabad

Identifier Type: -

Identifier Source: org_study_id

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