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Comparative clinical trial of efficacy and satisfaction of 2% gel lidocaine versus tetracaine/oxybuprocaine anesthetic eye drops in patients undergoing needing techniques in ophthalmology consultations.Anesthesia in Needling with Lidocaine (ANELI)

Phase 1
Recruiting
Conditions
Glaucoma
Therapeutic area: Diseases [C] - Eye Diseases [C11]
Registration Number
CTIS2023-505131-13-01
Lead Sponsor
Hospital Del Mar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients operated on glaucoma surgery with filtration ampoule who require the needling procedure in consultation, Over 18 years of age, who have understood and signed the informed consent.

Exclusion Criteria

Pregnant or breastfeeding patients, Patients who require needling in the operating room, Patients with cognitive impairment who do not understand the numerical rating scale in pain, Hearing loss that prevents patient collaboration, Anxiety disorder that prevents patient collaboration, Allergy to lidocaine, oxybuprocaine, or tetracaine, Patients who require needling in the operating room, Hypersensitivity to ester-type local anesthetics, other para aminobenzoic acid derivatives or to any of the excipients of Colirofta, Hypersensitivity to other amide-type local anesthetics or to any of the excipients of Ophtesic, Hypersensitivity to hypromelose gel

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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