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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02644603
Other study ID # H-ERAS-MRCT-1511
Secondary ID
Status Active, not recruiting
Phase N/A
First received December 15, 2015
Last updated June 24, 2017
Start date February 2016
Est. completion date June 2017

Study information

Verified date June 2017
Source Shanghai Zhongshan Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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).


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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 214
Est. completion date June 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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.

Locations

Country Name City State
China Zhongshan Hospital Shanghai Shanghai

Sponsors (5)

Lead Sponsor Collaborator
Shanghai Zhongshan Hospital Anhui Provincial Hospital, Eastern Hepatobiliary Surgery Hospital, RenJi Hospital, Subei People's Hospital of Jiangsu Province

Country where clinical trial is conducted

China, 

References & Publications (3)

Ni CY, Yang Y, Chang YQ, Cai H, Xu B, Yang F, Lau WY, Wang ZH, Zhou WP. Fast-track surgery improves postoperative recovery in patients undergoing partial hepatectomy for primary liver cancer: A prospective randomized controlled trial. Eur J Surg Oncol. 2013 Jun;39(6):542-7. doi: 10.1016/j.ejso.2013.03.013. Epub 2013 Apr 4. — View Citation

Sun HC, Qin LX, Lu L, Wang L, Ye QH, Ren N, Fan J, Tang ZY. Randomized clinical trial of the effects of abdominal drainage after elective hepatectomy using the crushing clamp method. Br J Surg. 2006 Apr;93(4):422-6. — View Citation

Wilmore DW, Kehlet H. Management of patients in fast track surgery. BMJ. 2001 Feb 24;322(7284):473-6. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Treatment related complications Number of adverse events that are related to treatment of each patients, and hospital readmission Up to 1 month since operation
Secondary Length of stay in hospital Length of stay in hospital (days) From the day a patient be hospitalized to the day discharged, up to 1 month.
Secondary Total hospitalization costs Total hospitalization costs (RMB yuan). From the day a patient be hospitalized to the day discharged, up to 1 month.
Secondary Preoperative and postoperative body weight Patient's body weight in kg. One day before operation, and the day patient discharged, up to 1 month.
Secondary Hemoglobin (Hb) test Hb/ALB/PRE-A(g/L), Hb in g/L. Day before operation and day 1/3/5 after operation.
Secondary Albumin (ALB) ALB in g/L. Day before operation and day 1/3/5 after operation.
Secondary PRE-Albumin (PRE-A) PRE-A in g/L Day before operation and day 1/3/5 after operation.
Secondary International Normalized Ratio (INR) INR in seconds. Day before operation and day 1/3/5 after operation.
Secondary Platelet (PLT) PLT in 10^9/L Day before operation and day 1/3/5 after operation.
Secondary Blood Urea Nitrogen (BUN) BUN in mmol/L Day before operation and day 1/3/5 after operation.
Secondary Blood Creatinine (sCr) sCr in umol/L Day before operation and day 1/3/5 after operation.
Secondary Alanine Transferase (ALT) ALT in U/L Day before operation and day 1/3/5 after operation.
Secondary Aspartate Transaminase (AST) AST in U/L Day before operation and day 1/3/5 after operation.
Secondary Interleukin-6 (IL-6) IL-6 in (pg/ml) Day before operation and day 1/3/5 after operation.
Secondary Interferon (IFN-?) IFN-?in pg/ml. Day before operation and day 1/3/5 after operation.
Secondary Tumor necrosis factor-a (TNF-a) TNF-ain pg/ml Day before operation and day 1/3/5 after operation.
Secondary Serum complement C3 and C4 in mg/dl Day before operation and day 1/3/5 after operation.
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