Skip to content

Meclizine Plasma Levels in Responders and Non-responders

Meclizine Plasma Levels in Responders and Non-responders

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04482985
Enrollment
50
Registered
2020-07-23
Start date
2020-09-01
Completion date
2021-09-01
Last updated
2020-07-23

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

Conditions

Meclizine, Seasickness

Keywords

Seasickness, Plasma Levels, Meclizine

Brief summary

Motion sickness is a debilitating condition that can effect many crew members. Meclizine has long been known as an effective anti motion sickness drug. The response to the drug is variable - some are responders, while others are resistant to the drug. The aim of the present study is to examine whether there is a correlation between meclizine plasma levels and clinical response.

Interventions

Meclzine is given to all study participants to prevent seasickness. Meclizine plasma levels are determined from both the meclizine responders and non responders group.

Sponsors

Medical Corps, Israel Defense Force
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Seasickness questioner (WIKER) score of 7. * Subjective functioning at 1 meter sea voyage - 5/10 and lower. * Subjects who were prescribed 25mg of meclizine. * Subjects who did not take any other drugs 48 prior to their participation in the study.

Exclusion criteria

* Known hearing loss or any vestibular impairment * Vertigo complains * Any ear infection * Use of Scopolamine based anti-seasickness drugs. * Use of meclizine 50mg.

Design outcomes

Primary

MeasureTime frameDescription
Meclizine plasma levels2 hours after meclizine administrationng/dl

Contacts

Primary ContactYoni Evgeni Gutkovich, M.D/Ph.D
gutkovichj@gmail.com+972526894497
Backup ContactDror Tal, Ph.D
tldror1@gmail.com+972549096080

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026