Kyung Hee university medical center
Seoul, South Korea
NCT Number: NCT03083522
The Purpose of this trial is to investigate the efficacy and safety of Ojeok-san(OJS) on Korean Patients With Cold Hypersensitivity in the Hands
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Notify Me19 year–59 year
Female
Interventional
Phase 3
Seoul, South Korea
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Usage: 3g, three times a day, each taken before or between meals Manufacturing company: HANPOONG PHARM & FOODS Co. Ltd.
Other names: OJS
Usage: 3g three times a day, each taken before or between meals Manufacturing company: HANPOONG PHARM & FOODS Co. Ltd.
Other names: corn starch
Time frame: At baseline, week 4, 8, 12
Time frame: At baseline, week 4, 8, 12
Time frame: At baseline, week 4, 8, 12
Time frame: At baseline, week 8
similar to the cold stimulation test
Time frame: every visit
Body temperature, blood pressure, pulse rate
Time frame: At screening visit, week 8
Levels of AST, ALT and r-GTP
Time frame: At screening visit, week 8
Levels of BUN and Cr
Time frame: At screening visit, week 8
Time frame: At week 4, 8, 12
Time frame: At screening visit
This questionnaire is a traditional medicine researcher self-developed questionnaire for collecting general symptoms of patients with Cold Hypersensitivity in the Hands and feet
Time frame: At screening visit
This tool is a traditional medicine researcher self-developed questionnaire of screening for patients with Cold Hypersensitivity in the Hands and feet In this trial, we will assess the validity of the tool.
Chan-Yong Jeon
Other
Efficacy and Safety of Ojeok-san on Korean Patients With Cold Hypersensitivity in the Hands and Feet - A Randomized, Double-blinded, Placebo Controlled, Multi-center Pilot Study
Acronym: OJS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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