A Sham Moxibustion Device and Masking Test

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0001934

Enrollment

Registered

2016-05-27

Start date

2016-05-27

Completion date

Unknown

Last updated

2019-03-11

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

Conditions

None listed

Interventions

Medical Device : Both moxibustion are composed of 33mm wide-40mm high bamboo, 20mm wide strainer and 50mm wide-5mm thickness styrofoam. - Real bamboo moxibustion : It is composed of 9g salt, 1.8g Arte

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: a subject who voluntarily agrees to participate and signs doesn't have an underlying disease.

Exclusion criteria

Exclusion criteria: 1. Subject who has a fear or side effects 2. Subject who has sensory impairment 3. Subject who is hypersensitive to fever 4. Subject who has skin lesions or wounds on the treatment region 5. Subject who has uncontrolled diabetes 6. Subject who has disability to communicate or fill out questionnaires 7. Pregnant or Subject who is judged as being not fit to moxibustion by a specialist

Design outcomes

Primary

Measure	Time frame
blinding evaluation;sensation difference between real moxibustion and sham moxibustion;observe adverse events	—

Secondary

Measure	Time frame
blinding difference by the experience of moxibustion;blinding difference by the reliability	—

Countries

Korea, Republic of

Contacts

Public ContactHyeryon kim

Dongguk University Bundang Oriental Hospital

6517275@hanmail.net

Outcome results