A Prospective Control Study of Cidan Capsule Combined With TACE in Hepatocellular Carcinoma
NCT ID: NCT02253511
Last Updated: 2014-10-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE4
400 participants
INTERVENTIONAL
2014-07-31
2017-07-31
Brief Summary
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Detailed Description
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Recently, a variety of Traditional Chinese Medicine combined with TACE for toxicity reduction and enhancing the efficacy have been investigated in the treatment of HCC. Cidan capsules are a formula containing more than ten types of plant extracts, including Rhizoma Curcumae (19%), Astragalus (19.6%), Cremastra appendiculata (9.8%), Salvia miltiorrhiza (9.8%), hive (9.8%) and Bombyx batryticatus (9.8%). Cidan has been clinically used for \>10 years as a safe and nontoxic antitumor drug. A number of studies have investigated the clinical application of TCMs for HCC, demonstrating that β-elemene, which is present in Rhizoma Curcumae and the main component of cidan, may inhibit the proliferation of HepG2 cells in a time- and dose-dependent manner. The results indicated that β-elemene exhibited positive effects on apoptosis and induced the cell cycle arrest of HepG2 cells in the G2/M phase, while Fas and Fas ligand expression levels were markedly increased.
In this prospective control study, we enroll such HCC patients experienced operation and were identifed with high risk of recurrence. After a preventive TACE, the eligible patients were divided into two groups. One group will accept Cidan therapy and another will not. Under a basis of large sample, the safty and efficacy of Cidan combined with TACE in HCC patients will be investigated and analysed.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Cidan capsule
Patients who undergone operation and TACE were administered 1.35 g cidan capsules (Weida Pharmaceutical Co., Ltd., Beijing, China) three times a day for 3 months.
Cidan capsule
Control group
Patients were only accepted operation and TACE.
No interventions assigned to this group
Interventions
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Cidan capsule
Eligibility Criteria
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Inclusion Criteria
* Liver function of Child-Pugh Class A or B.
* no intrahepatic and extrahepatic metastasis.
* Tumors had not invaded the portal vein, the hepatic vein trunk or the secondary branches.
* Patients undergone operation were confirmed to have the following high-risk recurrence factors:
Satellite nodules, Poor differentiation, Tumor diameter \> 5cm
* No evidence of coagulopathy: platelet count \> 50 × 109/L and a prolonged prothrombin time of \< 5 seconds.
* The patients would like to accept postoperative TACE.
Exclusion Criteria
* Impaired liver function with either clinically detected ascites, hepatic encephalopathy, serum albumin \< 25g/L or bilirubin \> 50micromol/L
* Renal impairment with creatinine \> 200micromol/L
* Severe concurrent medical illness persisting \> 6 weeks after hepatectomy
* History of other cancer
* Pregnant women
18 Years
75 Years
ALL
No
Sponsors
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Zheng Donghai
OTHER_GOV
Responsible Party
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Zheng Donghai
Vice-President of Beijing Weida Cancer Hospital of Chinese Traditional Medical Sciences
Principal Investigators
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Mengchao Wu, MD
Role: PRINCIPAL_INVESTIGATOR
Eastern Hepatobiliary Surgery Hospital
Locations
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Eastern Hepatobiliary Surgery Hospital
Shanghai, , China
Countries
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Central Contacts
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Facility Contacts
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References
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Zheng DH, Yang JM, Wu JX, Cheng SQ, Zhang SG, Wu D, Li AJ, Fu XH, Li X, Qi FC, Duan WH, Chen JH, Yang ZY, Liang L, Zeng JX, Zheng WD, Wu MC. Cidan Capsule in Combination with Adjuvant Transarterial Chemoembolization Reduces Recurrence Rate after Curative Resection of Hepatocellular Carcinoma: A Multicenter, Randomized Controlled Trial. Chin J Integr Med. 2023 Jan;29(1):3-9. doi: 10.1007/s11655-022-3537-4. Epub 2022 Aug 1.
Other Identifiers
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NST-CD
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
CD-2014
Identifier Type: -
Identifier Source: org_study_id
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