Clinical study of the anesthetic efficacy of 2% lidocaine gel versus tetracaine/oxybuprocaine anesthetic eye drops in patients operated on for glaucoma and undergoing needing techniques in outpatient surgery

Status

Not yet recruiting

Phases

Phase 4

Study type

Interventional

Source

EU CTIS

Registry ID

CTIS2023-505802-40-02

Enrollment

Registered

2024-02-19

Start date

Unknown

Completion date

Unknown

Last updated

2024-02-19

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

Conditions

glaucoma

Brief summary

Assessment of pain manifested by patients by numerical rating scale (NRS) from 0 to 10 /Average time spent on the procedure in both anesthetic treatment groups

Detailed description

Percentage of patients requiring re-anaesthesia in both treatment groups, Surgeon comfort/degree of patient cooperation: numerical rating scale (NRS) from 0 to 10., Percentage of patients requiring oral analgesia, Assessment of the visualization of the surgical field using a numerical scale from 0 to 5, with 5 being the best possible visualization

Interventions

DRUGOphtesic 20 mg/g

DRUGgel oftálmico en envase unidosis

DRUGCOLIROFTA ANESTÉSICO DOBLE 1 MG/ML + 4 MG/ML COLIRIO EN SOLUCIÓN

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Design outcomes

Primary

Measure	Time frame
Assessment of pain manifested by patients by numerical rating scale (NRS) from 0 to 10 /Average time spent on the procedure in both anesthetic treatment groups	—

Secondary

Measure	Time frame
Percentage of patients requiring re-anaesthesia in both treatment groups, Surgeon comfort/degree of patient cooperation: numerical rating scale (NRS) from 0 to 10., Percentage of patients requiring oral analgesia, Assessment of the visualization of the surgical field using a numerical scale from 0 to 5, with 5 being the best possible visualization	—

Countries

Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026