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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02299739
Other study ID # JS-CT-2013-02
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 2005
Est. completion date December 2013

Study information

Verified date November 2018
Source Jaseng Hospital of Korean Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Herb-induced liver injury is an important issue in musculoskeletal diseases where herbal medicine is most frequently used. The low prevalence of drug-induced liver injury (DILI) gives rise to the need for large-scale patient studies. We assessed the prevalence of liver injury of 6,894 musculoskeletal disease inpatients taking herbal medicine.


Description:

Herb-induced liver injury is an important issue in musculoskeletal diseases where herbal medicine is most frequently used. The low prevalence of drug-induced liver injury (DILI) gives rise to the need for large-scale patient studies. The objective of this study is to report on the incidence of liver injury from herbal medicine in musculoskeletal disease patients as large-scale studies are scarce.

Of 32,675 inpatients taking herbal medicine at 7 locations of a Korean medicine hospital between 2005 and 2013, we screened for liver injury in 6,894 patients with liver function tests (LFTs) at admission and discharge. LFTs included t-bilirubin, AST, ALT, and ALP. We assessed for risk factors for liver injury at discharge.

Participants received the most frequently used complementary and alternative medicine treatment contents (herbal medicine, acupuncture, pharmacopuncture, bee venom pharmacopuncture, and Chuna manipulation) administered to musculoskeletal disease patients at this hospital.


Recruitment information / eligibility

Status Completed
Enrollment 6894
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients admitted for at least one day who took herbal medicine and at least 2 LFTs during admittance.

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Herbal medicine
Herbal medicine was taken 3 times daily in dried powder (2g) and water-base decoction form (120ml) (Ostericum koreanum, Eucommia ulmoides, Acanthopanax sessiliflorus, Achyranthes bidentata, Psoralea corylifolia, Peucedanum japonicum, Cibotium barometz, Lycium chinense, Boschniakia rossica, Cuscuta chinensis, and Atractylodes japonica).
Procedure:
Acupuncture
Acupuncture treatment was administered 1-2 times daily using mainly Ah-shi points and local acupuncture points.
Pharmacopuncture
Select ingredients similar to those included in the oral herbal medicine (Ostericum koreanum, Eucommia ulmoides, Acanthopanax Sessiliflorus, Achyranthes bidentata, Psoralea corylifolia, Peucedanum japonicum, Cibotium barometz, Lycium chinense, Boschniakia rossica, Cuscuta chinensis, and Atractylodes japonica) were freeze dried into powder form after decoction, then diluted in normal saline and adjusted for acidity and pH to be used in injections. The pharmacopuncture injections were injected once daily to the amount of 1 cc and Ah-shi points and local acupuncture points (CPL, 1 cc, 26G x 1.5 syringe, Shinchang medical co., Korea).
Bee venom pharmacopuncture
Bee venom pharmacopuncture was applied after confirming a negative reaction to the hypersensitivity skin test. Diluted bee venom (saline:bee venom ratio, 10,000:1) was injected at 4-5 acupoints at the physician's discretion. Each acupuncture point was injected with approximately 0.2 cc to a total of 0.5-1 cc using disposable injection needles (CPL, 1 cc, 26G x 1.5 syringe, Shinchang medical co., Korea).
Chuna manipulation
Chuna was administered 3-5 times a week. Chuna is a Korean version of spinal manipulation that incorporates conventional spinal manipulation techniques for mobilization involving high-velocity, low amplitude thrusts to joints slightly beyond the passive range of motion and gentle force to joints within the passive range of movement.

Locations

Country Name City State
Korea, Republic of Jaseng Hospital of Korean Medicine Seoul Gangnam-Gu

Sponsors (1)

Lead Sponsor Collaborator
Jaseng Hospital of Korean Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Alanine aminotransferase (ALT) Participants were followed for the duration of hospital stay, an average of 4 weeks. Change from baseline (admission) in liver function test up to discharge (average 4 wks)
Primary Aspartate aminotransferase (AST) Participants were followed for the duration of hospital stay, an average of 4 weeks. Change from baseline (admission) in liver function test up to discharge (average 4 wks)
Primary Alkaline phosphatase (ALP) Participants were followed for the duration of hospital stay, an average of 4 weeks. Change from baseline (admission) in liver function test up to discharge (average 4 wks)
Primary Total bilirubin (TB) Participants were followed for the duration of hospital stay, an average of 4 weeks. Change from baseline (admission) in liver function test up to discharge (average 4 wks)
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