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Efficacy and Safety of Danggui-Sayuk-Ga-Osuyu-Saenggang-tang on Korean Patients With Cold Hypersensitivity in the Hands

Efficacy and Safety of Danggui-Sayuk-Ga-Osuyu-Saenggang-tang on Korean Patients With Cold Hypersensitivity in the Hands

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02645916
Enrollment
66
Registered
2016-01-05
Start date
2015-12-31
Completion date
2017-08-01
Last updated
2017-11-29

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

Conditions

Cold Hypersensitivity

Keywords

Cold Hypersensitivity in the Hands, Korean medicine, DSGOST

Brief summary

The Purpose of this trial is to investigate the efficacy and safety of Danggui-Sayuk-Ga-Osuyu-Saenggang-tang(DSGOST) on Korean Patients With Cold Hypersensitivity in the Hands

Interventions

DRUGDanggui-Sayuk-Ga-Osuyu-Saenggang-tang

Usage: 3g, three times a day, each taken before or between meals Manufacturing company: HANPOONG PHARM & FOODS Co. Ltd.

DRUGPlacebo: corn starch

Usage: 3g three times a day, each taken before or between meals Manufacturing company: HANPOONG PHARM & FOODS Co. Ltd.

Sponsors

Sangji University Oriental Medical Hospital
CollaboratorUNKNOWN
Semyung University Affiliated Oriental Medical Hospital
CollaboratorOTHER
Kyunghee University Medical Center
CollaboratorOTHER
Kyung Hee University Hospital at Gangdong
CollaboratorOTHER
DongGuk University
CollaboratorOTHER
Gachon University Gil Oriental Medical Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
19 Years to 59 Years
Healthy volunteers
No

Inclusion criteria

1. Female subjects aged 19 to 59 years have a complaint of CHH. 2. Patients must include at least one or more of the following symptoms: * Those who have the symptoms of CHH in normal temperature which most individuals feel no cold; * Those who have the symptoms of extremely cold hands in cold temperature exposure; * Those who are on the return to a warmer environment, the symptoms of cold hands is not completely rewarmed; 3. Those who have 4 cm or greater of VAS CHH score; 4. A thermal differences between the palm (PC8) and the upper arm (LU4) may be higher than 0.3℃; 5. Those who can comply with all study-related procedures, medications, and evaluations; 6. Given a written informed consent form.

Exclusion criteria

We will exclude patients who have taken 1. Patients with calcium antagonists or beta-blockers with the purpose of treating CHH; 2. Those who have one or more finger gangrene or ulceration; 3. Those who are diagnosed by hypothyroidism or currently medicated to thyroid drugs; 4. Those who are diagnosed by autoimmune disease or have a positive ANA test result; 5. Those who are diagnosed by carpal tunnel syndrome or have a positive Tinel and Phalen's tests; 6. Those who are diagnosed with cervical disc herniation or (malignant) tumor disease; 7. Those who are diagnosed with diabetes; 8. Those who are currently medicated to drugs that may affect to CHH symptoms, such as anticoagulants etc; 9. Those who have moderate level of liver dysfunction (each of AST, ALT greater than 100 IU/L) or kidney dysfunction (Cr 2.0mg/dL); 10. Those who do not (cannot) abide by treatment and follow up due to the mental illness such as behavior disorder, depression, anxiety neurosis, schizophrenia, or serious mental illness; 11. Those who are Diagnosed with moderate anemia and hematologic disorders (adult non-pregnant women hemoglobin (Hgb) level less than 7g/dL, hematocrit (Hct) level less than 26%, white blood cell (WBC) level greater than 11,000/mm3); 12. Those whose systolic blood pressure (SBP) 180mmHg or diastolic blood pressure (DBP) is greater than 100 mmHg based on average value of at least 2 measurements; 13. Those who are suspected arrhythmia that showing up on ECG, or diagnosed by heart diseases, such as, ischemic heart disease and so on; 14. Those who are addicted to alcohol or drugs; 15. Those who are pregnant (positive urine-HCG) or lactating or have the chances of pregnancy; 16. Those who are currently participated in other clinical trials; 17. Those who are able to understand and speak Korean; 18. Those who are judged to be inappropriate for the clinical study by the researchers.

Design outcomes

Primary

MeasureTime frame
Changes from baseline in visual analogue scaleAt baseline, week 2, 4, 6

Secondary

MeasureTime frameDescription
Changes from baseline in body temperatureAt baseline, week 2, 4, 6
Changes from baseline in clinical global impression(CGI)At baseline, week 2, 4, 6
Changes from baseline in WHOQoL-BREFAt baseline, week 2, 4, 6
Changes from baseline in cold stress testAt baseline, week 6similar to the cold stimulation test

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026