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INCIDENCE OF ALLERGIC CONTACT DERMATITIS FOLLOWING LIDOCAINE/PRILOCAINE CREAM APPLICATION: A CROSS-SECTIONAL STUDY

INCIDENCE OF ALLERGIC CONTACT DERMATITIS FOLLOWING LIDOCAINE/PRILOCAINE CREAM APPLICATION: A CROSS-SECTIONAL STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20260508003
Enrollment
50
Registered
2026-05-08
Start date
2026-05-09
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Allergic contact dermatitis from lidocaine and prilocaine cream Allergic contact dermatitis, lidocaine and prilocaine cream

Interventions

Patients with allergic contact dermatitis due to lidocaine/prilocaine confirmed by patch testing
Prevention
allergic contact dermatitis due to lidocaine/prilocaine

Sponsors

Strategic Wisdom and Research Institute, Srinakhanarinwirot University, Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age greater than or equal to 18 years 2.Patients who develop symptoms after application of topical anesthetic cream and are clinically suspected of allergic contact dermatitis from lidocaine/prilocaine cream by a physician 3.Willingness to participate in the study, able to undergo testing and follow-up, and provision of written informed consent

Exclusion criteria

Exclusion criteria: 1. Presence of any contraindication to patch testing, including at least one of the following: 1.1 Severe dermatitis 1.2 Use of immunosuppressive medications such as nonsteroidal anti-inflammatory drugs, corticosteroids, methotrexate, azathioprine, or cyclosporine within 4 weeks prior to enrollment 1.3 Dermatitis on the back or other test sites 1.4 History of ultraviolet therapy or sunburn at the test site within 21 days prior to enrollment 1.5 Use of topical corticosteroids at the test site within 14 days prior to enrollment 2. Pregnancy or breastfeeding 3. History of severe hypersensitivity reaction (anaphylaxis) to lidocaine/prilocaine cream 4. Known glucose-6-phosphate dehydrogenase (G6PD) deficiency

Design outcomes

Primary

MeasureTime frame
Incidence of allergic contact dermatitis and irritant contact dermatitis from lidocaine or prilocaine cream among patients with suspected symptoms 48, 72, 168 hour Patch testing

Secondary

MeasureTime frame
Allergens identified in patients with allergic contact dermatitis from lidocaine or prilocaine cream 48, 72, 168 hour Patch testing,Factors associated with the development of allergic contact dermatitis and irritant contact dermatitis from lidocaine or prilocaine cream at the beginning of study, Day7 Questionnaire

Countries

Thailand

Contacts

Public ContactSalinee Rojhirunsakool

Faculty of Medicine, Srinakharinwirot University

salinee.roj@gmail.com022041574

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026