Huaier Granule As Adjuvant Therapy for Colorectal Cancer After Radical Surgery

Last updated: June 14, 2016
Sponsor: Sixth Affiliated Hospital, Sun Yat-sen University
Overall Status: Trial Status Unknown

Phase

3

Condition

Colon Cancer

Rectal Cancer

Colon Cancer; Rectal Cancer

Treatment

N/A

Clinical Study ID

NCT02796820
zsly Huaier-2
  • Ages 18-75
  • All Genders

Study Summary

A randomized, paralleled control clinical study investigating Huaier Granule for prevention of recurrence and metastasis of colorectal cancer after radical surgery, to evaluate the efficacy and safety.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • The subjects volunteer to sign the informed consent;

  • Aged: 18 to 75 years old;

  • Colorectal cancer (AJCC-TNM, Stage Ⅰ, low-risk Stage Ⅱand Stage Ⅲ; Patients with Stage Ⅲ colorectal cancer refuse to postoperative adjuvant chemotherapy);

  • The diagnosis and colorectal cancer has been confirmed by pathological examinationafter radical surgery;

  • The liver and kidney function satisfies the following conditions within 15 days aftersurgery (excluding day 15): aspartate aminotransferase (AST), glutamic-oxalacetictransaminase (ALT), alkaline phosphatase (ALP)< 2 upper limit of normal (ULN), totalbilirubin ≤ 1.5 ULN, serum creatinine < 1.5 ULN; normal coagulation function;

  • Other laboratory tests meet the following requirements within 15 days after surgery (excluding day 15): white blood cells count ≥ 3.0×109/L, absolute neutrophil count ≥ 1.5×109/L, platelet count ≥ 100×109/L;

  • ECOG:0-2 points;

  • No other previous history of malignancy.

Exclusion

Exclusion Criteria:

  • Multiple primary cancer;

  • Not recover from the colorectal surgery;

  • Presence of organ, bone, or skin metastases;

  • Pregnant or lactating women;

  • Those with active bleeding due to various reasons;

  • Those with HIV infection or AIDS-associated diseases;

  • Those with severe acute and chronic diseases;

  • Those with severe diabetes;

  • Those with serious infectious diseases;

  • Those who can not take drugs by oral route;

  • Drug abusers or those with psychological or mental diseases that may interfere withstudy compliance;

  • Conditions that are considered not suitable for this study investigators.

Study Design

Total Participants: 230
Study Start date:
June 01, 2016
Estimated Completion Date:
June 30, 2018

Connect with a study center

  • Sixth Affiliated Hospital, Sun Yat-sen University

    Guangzhou, Guangdong 510655
    China

    Active - Recruiting

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