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Omnigen in Acute Chemical Eye Injuries (Omnigen)

Primary Purpose

Acute Chemical Eye Injuries

Status
Completed
Phase
Not Applicable
Locations
Kuwait
Study Type
Interventional
Intervention
vacuum-dehydrated amnion membrane (omnigen)
the lens loaded with Omnigen
Sponsored by
Farwaniya Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Chemical Eye Injuries focused on measuring amniotic membrane, chemical eye injury

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: acute chemical eye injury Exclusion Criteria: absent or shallow fornices symblepharon interfering with lens placement

Sites / Locations

  • Farwanyia Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

the lens loaded with Omnigen

Arm Description

patients with acute chemical eye injury treated with omnigen

Outcomes

Primary Outcome Measures

Epithelial healing
slit lamp examination with cobalt blue light after installing fluroscein drops
limbal ischaemia
slit lamp examination of the clock hours of vascularity around the limbususing both Due classification and Roper Hall

Secondary Outcome Measures

omnigen tolerability
questionnaire for the patients asking about discomfort sensation or the need to patch the eye

Full Information

First Posted
November 9, 2022
Last Updated
November 15, 2022
Sponsor
Farwaniya Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05618522
Brief Title
Omnigen in Acute Chemical Eye Injuries
Acronym
Omnigen
Official Title
Clinical Outcomes of Low Temperature Vacuum-dehydrated Amnion Membrane (Omnigen) in Treatment of Acute Chemical Eye Injuries
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
July 1, 2021 (Actual)
Primary Completion Date
July 1, 2022 (Actual)
Study Completion Date
September 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Farwaniya Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
evaluation of the role of Omnigen in acute chemical eye injuries
Detailed Description
prospective interventional study included patients with different degrees of acute chemical eye injuries were treated by Omnigen and followed up for one month

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Chemical Eye Injuries
Keywords
amniotic membrane, chemical eye injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
prospective
Masking
None (Open Label)
Allocation
N/A
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
the lens loaded with Omnigen
Arm Type
Other
Arm Description
patients with acute chemical eye injury treated with omnigen
Intervention Type
Procedure
Intervention Name(s)
vacuum-dehydrated amnion membrane (omnigen)
Other Intervention Name(s)
application of amnilenz
Intervention Description
applying the lens loaded with Omnigen on the cornea
Intervention Type
Device
Intervention Name(s)
the lens loaded with Omnigen
Intervention Description
the lens loaded with Omnigen
Primary Outcome Measure Information:
Title
Epithelial healing
Description
slit lamp examination with cobalt blue light after installing fluroscein drops
Time Frame
1 week
Title
limbal ischaemia
Description
slit lamp examination of the clock hours of vascularity around the limbususing both Due classification and Roper Hall
Time Frame
1 week
Secondary Outcome Measure Information:
Title
omnigen tolerability
Description
questionnaire for the patients asking about discomfort sensation or the need to patch the eye
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: acute chemical eye injury Exclusion Criteria: absent or shallow fornices symblepharon interfering with lens placement
Facility Information:
Facility Name
Farwanyia Hospital
City
Al Farwānīyah
State/Province
Farwanyia
ZIP/Postal Code
13001
Country
Kuwait

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Omnigen in Acute Chemical Eye Injuries

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