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Study of Effectiveness of Mexyn-A

Proof of Concept of MEXYN-A

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00568204
Acronym
Mexyn-A
Enrollment
279
Registered
2007-12-05
Start date
2002-03-31
Completion date
2005-09-30
Last updated
2013-10-17

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

Conditions

Pruritus

Keywords

pruritus, itching, mexyn-a, clearitch, magicool-plus

Brief summary

Atomised Methoxymethane-in-Aqua (MEXYN-A) a new topical self-chilled, non-steroidal, non-flammable, pressurised spray which embodies in one simultaneous application, most of the currently recognised and effective chemical, mechanical and thermal anti-pruritic therapies and hydrotherapy.

Detailed description

The primary clinical endpoint was to establish MEXYN-A efficacy and safety in abolishing or reducing pruritus related to cutaneous diseases, insect bites and poison ivy, within few seconds of the application. The secondary endpoint was to measure the itch free period as a result of the new intervention.

Interventions

DEVICEMexyn-A

Atomised topical self-chilled pressurised spray

Sponsors

Evangelical Synod Medical Centre
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients suffering from severe itching due to : Atopic Dermatitis, contact dermatitis, psoriasis, urticaria, xerosis, prickly heat, genital pruritus, chicken pox, aquagenic pruritus, lichen planus, poison ivey, insect bites. * Past experience with the use of at least one conventional medication for pruritus or conventional medication for the same disorder patients suffered.

Exclusion criteria

* Patients who have taken any anti-pruritic drug during the month prior to participation. * Patients who have taken drugs for any reason for 2 days prior to participating in the study.

Design outcomes

Primary

MeasureTime frame
Treating Pruritusthree days

Secondary

MeasureTime frame
measuring itch-free period after applying the new treatment, effect on sleep disturbancethree days

Countries

Egypt

Outcome results

None listed

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