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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02348229
Other study ID # 2013-212
Secondary ID
Status Completed
Phase N/A
First received January 17, 2015
Last updated January 27, 2015
Start date September 2013
Est. completion date October 2014

Study information

Verified date January 2015
Source First Hospital of Jilin University
Contact n/a
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The investigators designed a prospective randomized, controlled clinical trial then recruited 149 consecutive advanced gastric cancer patients. Further divided into a ERAS group (n=73) and a conventional pathway group (n=76). Surgical technique in both groups was same laparoscopic-assisted gastrectomy with D2 lymphadenectomy. Compared outcomes included clinical parameters and serum indicators.


Description:

Enhanced recovery after surgery combined with laparoscopic-assisted gastrectomy was successfully carried out in this study. Recovery parameters such as the length of time to return to normal diet,mean hospital stay (d) were recorded.


Recruitment information / eligibility

Status Completed
Enrollment 149
Est. completion date October 2014
Est. primary completion date September 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

1. Age 18-75 years old

2. Diagnosis confirmed by the endoscopic biopsy and total-body CT scan

3. No history of the chronic renal disease ,chronic liver disease, cardiopulmonary dysfunction, ASA score?3

4. No neoadjuvant chemotherapy and radiotherapy

5. No digestive obstruction and distant metastasis

Exclusion Criteria:

1. Conversion to open gastrectomy

2. A large amount of bleeding leading(>500ml)

3. Patients withdrew their consent

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
ERAS protocols
Normal meal allowed until 6 h before surgery and Carbohydrate drink until 2 h before surgery
ERAS protocols
No bowel preparation
ERAS protocols
No nasogastric placement; if used, remove on the 1st postoperative day
ERAS protocols
Vasoactive drugs used if need be
ERAS protocols
Temperature management
ERAS protocols
Intra-abdominal drains not to be used
ERAS protocols
Intraperitoneal Ropivicaine infusion
ERAS protocols
On the 1st postoperative day Nasogastric catheter removed /Urinary catheter removed. Oral non-opioid analgesia/Drinking 0.5L liquid. Active mobilisation
ERAS protocols
On the 2nd postoperative day:Drains removed Oral diet was initiated
ERAS protocols
3-4th postoperative day: Stop oral non opioid analgesia
ERAS protocols
On the5-6th postoperative day Check discharge criteria
conventional pathway group
No solid foods at dinner before surgery and no liquids 12 h before surgery. Routine bowel preparation Nasogastric placement on the morning of surgery
conventional pathway group
Routine use of anesthesia medicine. Standard 5-trocar laparoscopy-assisted procedure. I.V. fluids not restricted (Ringer's lactate 20 ml/kg in the first hour, then at the rate of 10-12 ml/kg/h) Routine use of abdominal drainage tubes and placement of catheters.
conventional pathway group
1st postoperative day: Keep Nasogastric catheter Removal of urinary catheter Opioid analgesic by intramuscular injection Parenteral nutrition until flatus. I.V. fluids not restricted Mobilization in bed
conventional pathway group
2nd postoperative day Patient is advised to get out of bed until 24-48h after surgery
conventional pathway group
3-4th postoperative day: Remove nasogastric tube after flatus Oral liquids started. Encouraged to walk in the ward.
conventional pathway group
5-6th postoperative day:Oral diet was changed from liquids to semi-fluids and normal food. Drains removed

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
First Hospital of Jilin University

Outcome

Type Measure Description Time frame Safety issue
Primary Compartition of postoperative hospital stay up to 30 days after the operation No
Secondary Change from baseline in C-Reactive Protein( CRP) and visceral proteins level 1day before and 1-5days after operation baseline and 5 days No
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