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Examination to identify the relationship between temperature/soaking time of the Ivermectin whole body method and transition to horny layer

Examination to identify the relationship between temperature/soaking time of the Ivermectin whole body method and transition to horny layer - Ivermectin partial body bath test for healthy adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011016
Enrollment
10
Registered
2013-06-22
Start date
2013-06-21
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

scabies

Interventions

Prepare the Ivermectin whole body bath solution by melting a half tablet of Stromectol&amp
reg
3mg per 10 liters of hot water (in which baby bath agent is added). This solution is used for partial body bathing. Partial body bath test is conducted five times
two of them are for investigating soaking time
two of them are for investigating bath agent
one of them is for identifying the effect of elapsed time after bathing.

Sponsors

Tokyo University of Science
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Healthy and over age of 20 2) Have written consent on subjects' free will after being completely explained about this study

Exclusion criteria

Exclusion criteria: 1) The patient who has an obstacle in the barrier of the skin according to a skin disorder 2) Those who have the following diseases in the past or the present - Liver disease - The disease considered to affect a test result by a doctor in attendance in addition to this, or the disease considered that medication of ivermectin brings about a disadvantage 3) The superfluous ingestion person of the coffee containing caffeine, or a drink (>8 cup / day) 4) The abuse person of medicine or alcohol 5) The addict of an illegal drug 6) The woman who offered the blood of 400mL within the man and woman who offered the blood of 200mL within four weeks before the examination or the man who offered the blood of 400mL within 12 weeks, and 16 weeks 7) Those who participated in four weeks to the clinical test using other investigational new drugs before this start of test 8) Those who have an anamnesis of hypersensitivity in the ingredient of a Stromectol® Tablets or the charge of baby purification (Pigeon, Inc.) 9) The woman, the child below 15 km who have become pregnant 10) Those whom the examination doctor in attendance judged to be unsuitable as a subject 11) Those who have used medication within a week

Design outcomes

Primary

MeasureTime frame
Effects of difference in temperature/ soaking time/ bath agent on the concentration of Ivermectin transited to horny layer

Secondary

MeasureTime frame
Identification of adverse events by examined drug

Countries

Japan

Contacts

Public ContactMasayo Komoda

Tokyo University of Science Faculty of Pharmaceutical Sciences

komo1207@rs.noda.tus.ac.jp04-7121-4134

Outcome results

None listed

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