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Experimental study of the serum and horny layer concentration shift in Ivermectin bath method

Experimental study of the serum and horny layer concentration shift in Ivermectin bath method - Ivermectin bath trail for healthy adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000013068
Enrollment
6
Registered
2014-02-04
Start date
2013-11-18
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

After preparing Ivermectin bath solution that 4 tablets of Stromectol put into 150 liters of hot water with baby bath agent, volunteer takes the bath for from 5 to 15minutes. Then, the state of the sk

Sponsors

Tokyo University of Science
Lead Sponsor
Kikkoman General Hospital
Collaborator

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 during pregnancy or potential pregnancy, and breast-feeding 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
-The concentration of Ivermectin in horny layer -The concentration of Ivermectin in blood

Secondary

MeasureTime frame
-The concentration of Ivermectin in the bath solution -Toxic Epidermal necrosis -Stevens-Johnson syndrome -Impairment of liver function -Other adverse events

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