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A paired, randomized, double-blind, placebo-controlled trial of EMLA cream (eutectic mixture of local anesthetics) for primary localized cutaneous amyloidosis.

A paired, randomized, double-blind, placebo-controlled trial of EMLA cream (eutectic mixture of local anesthetics) for primary localized cutaneous amyloidosis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20170928005
Enrollment
15
Registered
2017-09-28
Start date
2017-10-01
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

primary localized cutaneous amyloidosis symmetry both legs primary localized cutaneous amyloidosis lichen amyloidosus EMLA topical anesthetic pruritus itch

Interventions

apply EMLA cream at one side of leg (leg A),apply placebo cream at one side of leg (leg B)
Experimental Drug,Placebo Comparator No treatment
EMLA cream,placebo (hydrophilic cream)

Sponsors

none
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 18-60 years old primary localized cutaneous amyloidosis at both legs symmetry

Exclusion criteria

Exclusion criteria: 1.previous laser within 3 months or use topical treatment within 1 month 2.other skin diseases 3.pregnancy or lactation 4.history of allergy to anesthesic agents or amide derivative 5.glucose-6-phosphatase defiency (G6PD) 6.using nitric oxide, sulfonamides, dapsone, metoclopramide, nitrofurantoin, beta-blockers drug 7.arrhythmia 8.immunodeficiency 9.psychiatric problem

Design outcomes

Primary

MeasureTime frame
pruritus 0 wk, 2 wk, 4 wk, 8 wk visual analog scale (VAS)

Secondary

MeasureTime frame
volume of elevated lesion 0 wk, 2 wk, 4 wk, 8 wk Antera 3D

Countries

Thailand

Contacts

Public ContactPravit Asawanonda

Faculty of Medicine, Chulalongkorn University

fibrosis@gmail.com022564253

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026