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Preservative-free Topical Anesthetics for Post-PRK Pain

Primary Purpose

Myopia

Status
Completed
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Preservative-free Benoxinate hydrochloride 0.4% (Benoxidia unit-dose vials [UD], Orchidia pharmaceutical Ind., Egypt)
Preservative-free Sodium hyaluronate 0.2% (Polyfresh unit-dose vials [UD], Orchidia pharmaceutical Ind., Egypt).
Sponsored by
Assiut University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myopia focused on measuring Post-PRK pain, Preservative-free topical anesthetics, Single-step PRK

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Patients who are candidate for PRK surgery with Myopia up to - 6 diopters or myopic astigmatism up to - 4 diopters. Corneal thinnest pachymetry of 500 µm Residual stromal bed more than 350 µm after epithelial ablation. Exclusion Criteria: Patients with Corneal scars or dry eye disease, Past ocular surgery, History of contact lens wear, Systemic diseases such as diabetes mellitus and autoimmune diseases, History of oral analgesics abuse.

Sites / Locations

  • Tiba Eye Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Preservative-free topical anesthetics group

Preservative-free artificial tears group

Arm Description

Patients in this group had the standard post-PRK treatment regimen in addition to the prescription of preservative-free topical anesthetics for pain control following single-step transepithelial PRK surgery in one eye.

Patients in this group had the standard post-PRK treatment regimen in addition to the prescription of preservative-free artificial tears as a placebo following single-step transepithelial PRK surgery in the other eye.

Outcomes

Primary Outcome Measures

Postoperative pain score on the verbal rating scale (VRS)
The doctor asks the patient to choose the word that best describes his/her pain and then gives it a score from zero to 4 (Zero for no pain, 1 for mild pain, 2 for moderate pain, 3 for severe pain and 4 for unbearable pain).
Postoperative pain score on the visual analogue scale (VAS)
The patient is asked to rate his/her pain by choosing a number on a scale from zero to 10 considering zero as no pain and 10 as worst possible pain.

Secondary Outcome Measures

Corneal epithelial healing duration
Time for the corneal epithelium to heal reported in days after PRK surgery
Endothelial cell density (ECD)
Specular microscopy was used to assess endothelial cell count before and after PRK surgery

Full Information

First Posted
January 30, 2023
Last Updated
May 23, 2023
Sponsor
Assiut University
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1. Study Identification

Unique Protocol Identification Number
NCT05733741
Brief Title
Preservative-free Topical Anesthetics for Post-PRK Pain
Official Title
Preservative-free Topical Anesthetics for the Management of Postoperative Pain Following Photorefractive Keratectomy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
January 30, 2023 (Actual)
Primary Completion Date
April 15, 2023 (Actual)
Study Completion Date
April 15, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Assiut University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this interventional comparative study is to assess the efficacy and safety of a novel regimen of preservative-free unit-dose topical anesthetics for controlling early postoperative pain following single-step transepithelial PRK surgery. The main research questions to answer are: Question 1: Are topical anesthetics effective in reducing post-PRK pain? Question 2: Are short-term topical anesthetics toxic to the cornea? Question 3: How to prevent abuse of topical anesthetics by patients at home? Participants were planned to undergo a bilateral single-step transepithelial PRK surgery to correct their refractive errors and received a standard post-PRK treatment regimen for both eyes. Additionally, one eye was offered a preservative-free topical anesthetic as an experimental group and the other eye was offered a preservative-free artificial tear as a control group.
Detailed Description
Photorefractive keratectomy (PRK) is a well-established surface ablation procedure for correction of refractive errors which involves the removal of corneal epithelium in a large diameter usually more than 6 mm followed by stromal ablation. Early postoperative pain within the first few days after surgery is one of the commonest complications reported after PRK. The classic postoperative treatment includes the prescription of topical antibiotics and frequent preservative-free lubricants to accelerate epithelial healing. The current treatment regimens also includes topical steroids, topical non-steroidal anti-inflammatory drugs (NSAID) and oral NSAID to reduce inflammation and post-PRK pain. Earlier studies suggested that topical anesthetics in diluted concentrations and fractional doses didn't delay corneal epithelial regeneration after PRK but their use didn't gain popularity because of problems with topical formulation, stability and preservation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myopia
Keywords
Post-PRK pain, Preservative-free topical anesthetics, Single-step PRK

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Preservative-free topical anesthetics group
Arm Type
Experimental
Arm Description
Patients in this group had the standard post-PRK treatment regimen in addition to the prescription of preservative-free topical anesthetics for pain control following single-step transepithelial PRK surgery in one eye.
Arm Title
Preservative-free artificial tears group
Arm Type
Placebo Comparator
Arm Description
Patients in this group had the standard post-PRK treatment regimen in addition to the prescription of preservative-free artificial tears as a placebo following single-step transepithelial PRK surgery in the other eye.
Intervention Type
Drug
Intervention Name(s)
Preservative-free Benoxinate hydrochloride 0.4% (Benoxidia unit-dose vials [UD], Orchidia pharmaceutical Ind., Egypt)
Intervention Description
For each patient, one eye was treated with preservative-free Benoxinate hydrochloride 0.4%. The prescribed regimen comprises of the instillation of one drop immediately, 2, 4, 6 and 8 hours after the end of surgery. Every patient was given 5 UD vials only of preservative-free Benoxinate hydrochloride 0.4% at each follow up visit for the next postoperative day usage administered 5 times daily (every 3 hours while awake) for the first 3 postoperative days giving clear instructions to immediately discard the vial after single use.
Intervention Type
Drug
Intervention Name(s)
Preservative-free Sodium hyaluronate 0.2% (Polyfresh unit-dose vials [UD], Orchidia pharmaceutical Ind., Egypt).
Intervention Description
The other eye was treated with preservative-free Sodium hyaluronate 0.2%. The prescribed regimen comprises of the instillation of one drop immediately, 2, 4, 6 and 8 hours after the end of surgery. Every patient was given 5 UD vials only of preservative-free Sodium hyaluronate 0.2% at each follow up visit for the next postoperative day usage administered 5 times daily (every 3 hours while awake) for the first 3 postoperative days giving clear instructions to immediately discard the vial after single use.
Primary Outcome Measure Information:
Title
Postoperative pain score on the verbal rating scale (VRS)
Description
The doctor asks the patient to choose the word that best describes his/her pain and then gives it a score from zero to 4 (Zero for no pain, 1 for mild pain, 2 for moderate pain, 3 for severe pain and 4 for unbearable pain).
Time Frame
1 week
Title
Postoperative pain score on the visual analogue scale (VAS)
Description
The patient is asked to rate his/her pain by choosing a number on a scale from zero to 10 considering zero as no pain and 10 as worst possible pain.
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Corneal epithelial healing duration
Description
Time for the corneal epithelium to heal reported in days after PRK surgery
Time Frame
1 week
Title
Endothelial cell density (ECD)
Description
Specular microscopy was used to assess endothelial cell count before and after PRK surgery
Time Frame
from preoperative to 1 month postoperative.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients who are candidate for PRK surgery with Myopia up to - 6 diopters or myopic astigmatism up to - 4 diopters. Corneal thinnest pachymetry of 500 µm Residual stromal bed more than 350 µm after epithelial ablation. Exclusion Criteria: Patients with Corneal scars or dry eye disease, Past ocular surgery, History of contact lens wear, Systemic diseases such as diabetes mellitus and autoimmune diseases, History of oral analgesics abuse.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mahmoud Abdel-Radi, MD
Organizational Affiliation
Assiut University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tiba Eye Center
City
Assiut
ZIP/Postal Code
71516
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36207168
Citation
Steigleman WA, Rose-Nussbaumer J, Al-Mohtaseb Z, Santhiago MR, Lin CC, Pantanelli SM, Kim SJ, Schallhorn JM. Management of Pain after Photorefractive Keratectomy: A Report by the American Academy of Ophthalmology. Ophthalmology. 2023 Jan;130(1):87-98. doi: 10.1016/j.ophtha.2022.07.028. Epub 2022 Oct 4.
Results Reference
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Preservative-free Topical Anesthetics for Post-PRK Pain

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