Comparison of skin prick test devices with different applied forces for skin prick testing

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

TCTR

Registry ID

TCTR20220627004

Enrollment

Registered

2022-06-27

Start date

2022-04-19

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

Healthy participant Skin prick test Diagnostic Plastic Device Sensitivity Performance Pain Histamine

Interventions

The performance of ALK lancet under three different applied forces (30, 45 and 60 g) using a home-made force-controlled device (Applicator). ,The performance of Feather lancet under three different ap

Experimental Procedure/Surgery,Experimental Procedure/Surgery,Experimental Device,Experimental Device,Active Comparator Device

ALK lancet,Feather Lancet,CU Test-1,CU Test-2,Manual ALK and needle

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Healthy subjects in the age of 18 years and over were eligible for enrolment in the study.

Exclusion criteria

Exclusion criteria: The use of antihistamines within the last 7 days of the test, obvious skin lesions, dermographism or atopic dermatitis, a fear of needle, any history of severe allergy, pregnancy, or the use of drugs.

Design outcomes

Primary

Measure	Time frame
Skin prick test 15 min The mean wheal size was calculated from the average of the lengths along the longitudinal and orthogonal axes of the wheal	—

Secondary

Measure	Time frame
safety 15 min local adverse effect	—

Countries

Thailand

Contacts

Public ContactPantipa Chatchatee

Chulalongkorn University

pantipa.c@chula.md022564971

Outcome results

None listed

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