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Topical Ice-therapy for Intravitreal Injections

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Completed

Conditions

Injection Site Irritation
Anesthesia; Hypothermia

Treatments

Other: Ice-therapy
Other: No Ice-therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05269823
OPH-2022-30605

Details and patient eligibility

About

Purpose: To examine the difference in patient's pain experience in the setting of intravitreal anti-VEGF injections with pretreatment of topical ice-therapy compared with no-ice.

Enrollment

42 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All patients aged 18 or older evaluated by a single retina specialist at the University of Minnesota Department of Ophthalmology with a clinical indication necessitating an anti-VEGF intravitreal injection

Exclusion criteria

  • N/A

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

42 participants in 2 patient groups, including a placebo group

Ice-therapy
Active Comparator group
Description:
Ice therapy will be provided prior to the provision of the intravitreal injection
Treatment:
Other: Ice-therapy
No Ice-therapy
Placebo Comparator group
Description:
No ice therapy will be provided prior to the provision of the intravitreal injection
Treatment:
Other: No Ice-therapy

Trial contacts and locations

1

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Central trial contact

Jade Moon, MD

Data sourced from clinicaltrials.gov

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