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Efficacy of CGS-1 in Migraine Female Volunteers: Randomized, Single-blind, Placebo-controlled, Crossover Trial

Efficacy of CGS-1 in Migraine Female Volunteers: Randomized, Single-blind, Placebo-controlled, Crossover Trial - Efficacy of CGS-1 in Migraine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000028919
Enrollment
40
Registered
2017-09-24
Start date
2017-09-25
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

Migraine

Interventions

Apply the CGS-1 for forehead for 2 hours. Apply the placebo for forehead for 2 hours.

Sponsors

Kao Corporation
Lead Sponsor
Tokyo Clinic
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1)Women aged 20-49. 2)Subjects with migraine without aura experience three to five migraine per month. 3)Subjects with lucidity and no intellectual disability can communicate. 4)Written informed consent. 5)If migraine and tension type headache are merged, the subjects can distinguish between the two.

Exclusion criteria

Exclusion criteria: 1)Subjects with migraine with aura 2)Subjects with the headache without migraine 3)Subjects with taking triptan medicine. 4)Subjects with the hemicrania continua. 5)Subjects with pregnancies and lactations. 6)Subjects with atopic dermatitis. 7)Subjects with vulnerable to skin irritation by menthol or alcohol. 8)Subjects deemed inappropriate to participate in this study by the principle investigator

Design outcomes

Primary

MeasureTime frame
Change in NRS (Numerical Rating Scale) from the start of the test to 30 minutes later.

Secondary

MeasureTime frame
1)Change in NRS (Numerical Rating Scale) at 60 minutes, 120 minutes and 180 minutes after the start of the test. 2)Changes in daily disability assessment HIT (Headache Impact Test) - 6

Countries

Japan

Contacts

Public ContactNobuyasu Kimura

Tokyo Clinic Pain Clinic of Internal Medicines

kimukimu1234@hotmail.co.jp03-3516-7151

Outcome results

None listed

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