Enrolling by invitation NCT06962709
Studying Warmed Lidocaine for Increased Analgesic Effect During Intravitreal Injections
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Warmed lidocaine.
- Who it may be relevant to
- Registry conditions: Pain Intensity Assessment, Pain Management. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Comparing the Anesthetic Effect of Warmed Lidocaine to Room Temperature Lidocaine When Applied Topically for Intravitreal Injections
Overview
Investigating whether warmed lidocaine increases analgesic effect for intravitreal injections
Interventions
- Other Warmed lidocaine
Lidocaine warmed to 98 F
Primary outcome measures
- Pain Rating [Time frame: immediately after the intervention]
Eligibility criteria
Inclusion criteria
- Receiving intravitreal injection for any indication
Exclusion criteria
- Previous participant in study
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Other
Study locations
United States · 1 center
- University Hospital - Mason Eye Clinic — Columbia
Identifiers
NCT: NCT06962709 · 2090898