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Comparative investigation of clinical utility of EMLA cream and lidocaine tape at laser therapy

Comparative investigation of clinical utility of EMLA cream and lidocaine tape at laser therapy - Comparative investigation of clinical utility of EMLA cream and lidocaine tape at laser therapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011515
Enrollment
40
Registered
2013-08-19
Start date
2013-08-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Angioma, nevus, mole, seborrheic keratosis, senile lentigo, tattoo

Interventions

A half side test of EMLA cream and lidocaine tape

Sponsors

Juntendo University School of Medicine
Lead Sponsor
Seisho Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who have angioma, nevus, tattoo, mole, seborrheic keratosis, or senile lentigo. Patients who was diagnosed to receive laser therapy Patients who obtained the document voluntary consent of the patient himself after receiving a sufficient explanation upon participation in this study , on a full understanding

Exclusion criteria

Exclusion criteria: Patients who have allergy of Anilide anesthetic Patients who have alcoholism or drug addiction Patients who have liver disease, kidney disease, or heart disease Patients who have eczema, dermatitis or scar at the region that will be applied investigational drugs Patients who received medication that affect drug evaluation (example; topical anesthesia, general anesthesia, sedative, anxiolytic, antipyretic analgesic, corticosteroid, antipruritic drug, convergence drug, opium alkaloid drug, coca alkaloid drug, Synthetic narcotics ) Patients who is desensitization Patients who participated in other clinical study within 6 months before this study Patients who is participating other clinical study at present Patients who have already participated in this study Patients who is pregnant or lactating Patients whom the doctor responsible for this study judged unfit for this study

Design outcomes

Primary

MeasureTime frame
VAS

Secondary

MeasureTime frame
Questionnaire survey

Countries

Japan

Contacts

Public ContactRica Tanaka

Juntendo University School of Medicine Department of Plastic and Reconstructive surgery

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026