Effect of Enhanced Recovery After Surgery(ERAS) After Liver Resection for Primary Liver Cancer

Sponsor
Shanghai Zhongshan Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT02644603
Collaborator
Eastern Hepatobiliary Surgery Hospital (Other), RenJi Hospital (Other), Anhui Provincial Hospital (Other), Subei People's Hospital of Jiangsu Province (Other)
214
1
2
16
13.4

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate Enhanced Recovery After Surgery(ERAS) protocol versus conventional treatment on patients who underwent liver resection for hepatocellular carcinoma(HCC).

Condition or Disease Intervention/Treatment Phase
  • Procedure: Enhanced Recovery After Surgery
N/A

Detailed Description

212 patients are randomly recruited from inpatients of Shanghai Zhongshan Hospital, Eastern Hepatobiliary Surgery Hospital, RenJi Hospital, Anhui Provincial Hospital, Subei People's Hospital of Jiangsu Province and Affiliated Tumor Hospital of Nantong University from February 2016 to July 2016. Randomly assigned about half of the patients to receive Enhanced Recovery After Surgery(ERAS) protocol and the other half to receive conventional treatment. Evaluate the safety and efficacy of the ERAS protocol.

Study Design

Study Type:
Interventional
Actual Enrollment :
214 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Safety and Efficacy of the Enhanced Recovery After Surgery(ERAS) After Liver Resection for Primary Liver Cancer: a Multicenter, Randomized, Controlled Clinical Study
Actual Study Start Date :
Feb 1, 2016
Actual Primary Completion Date :
Dec 1, 2016
Anticipated Study Completion Date :
Jun 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Enhanced Recovery After Surgery

Patients underwent ERAS protocol

Procedure: Enhanced Recovery After Surgery
Before operation: Preoperative optimization of organ function, No preoperative bowel preparation, Prohibit eating 6h, drinking water 2h before operation, Oral rehydration before operation. In operation: Optimized combined anesthesia, Minimal invasive operations, Normothermia, Minimal use of tubes and drains. After operation: Postoperative analgesia and antiemetic, Early mobilization, Oral nutrition, Early and scheduled mobilization.
Other Names:
  • Fast Track Surgery
  • No Intervention: Conventional Treatment

    Patients underwent conventional treatment

    Outcome Measures

    Primary Outcome Measures

    1. Treatment related complications [Up to 1 month since operation]

      Number of adverse events that are related to treatment of each patients, and hospital readmission

    Secondary Outcome Measures

    1. Length of stay in hospital [From the day a patient be hospitalized to the day discharged, up to 1 month.]

      Length of stay in hospital (days)

    2. Total hospitalization costs [From the day a patient be hospitalized to the day discharged, up to 1 month.]

      Total hospitalization costs (RMB yuan).

    3. Preoperative and postoperative body weight [One day before operation, and the day patient discharged, up to 1 month.]

      Patient's body weight in kg.

    4. Hemoglobin (Hb) test Hb/ALB/PRE-A(g/L), [Day before operation and day 1/3/5 after operation.]

      Hb in g/L.

    5. Albumin (ALB) [Day before operation and day 1/3/5 after operation.]

      ALB in g/L.

    6. PRE-Albumin (PRE-A) [Day before operation and day 1/3/5 after operation.]

      PRE-A in g/L

    7. International Normalized Ratio (INR) [Day before operation and day 1/3/5 after operation.]

      INR in seconds.

    8. Platelet (PLT) [Day before operation and day 1/3/5 after operation.]

      PLT in 10^9/L

    9. Blood Urea Nitrogen (BUN) [Day before operation and day 1/3/5 after operation.]

      BUN in mmol/L

    10. Blood Creatinine (sCr) [Day before operation and day 1/3/5 after operation.]

      sCr in umol/L

    11. Alanine Transferase (ALT) [Day before operation and day 1/3/5 after operation.]

      ALT in U/L

    12. Aspartate Transaminase (AST) [Day before operation and day 1/3/5 after operation.]

      AST in U/L

    13. Interleukin-6 (IL-6) [Day before operation and day 1/3/5 after operation.]

      IL-6 in (pg/ml)

    14. Interferon (IFN-γ) [Day before operation and day 1/3/5 after operation.]

      IFN-γin pg/ml.

    15. Tumor necrosis factor-α (TNF-α) [Day before operation and day 1/3/5 after operation.]

      TNF-αin pg/ml

    16. Serum complement [Day before operation and day 1/3/5 after operation.]

      C3 and C4 in mg/dl

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Diagnosed with HCC with indications for surgery

    • Without any surgical contraindications

    • Under went open liver resection

    • Operation ranges less than 4 hepatic segments

    • Informed consent

    Exclusion Criteria:
    • Not suitable for surgery

    • Benign lesions or other lesions proved by pathology

    • Surgical procedure changed during operation or combined evisceration

    • Refused to participate or drop out

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Zhongshan Hospital Shanghai Shanghai China 200032

    Sponsors and Collaborators

    • Shanghai Zhongshan Hospital
    • Eastern Hepatobiliary Surgery Hospital
    • RenJi Hospital
    • Anhui Provincial Hospital
    • Subei People's Hospital of Jiangsu Province

    Investigators

    • Study Director: Jian Zhou, MD, PhD, Shanghai Zhongshan Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Shanghai Zhongshan Hospital
    ClinicalTrials.gov Identifier:
    NCT02644603
    Other Study ID Numbers:
    • H-ERAS-MRCT-1511
    First Posted:
    Jan 1, 2016
    Last Update Posted:
    Jun 27, 2017
    Last Verified:
    Jun 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Keywords provided by Shanghai Zhongshan Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 27, 2017