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Clinical Trials/NCT02649348
NCT02649348
Completed
Not Applicable

Effects of Pre-operative Prehabilitation on the Clinical Outcomes of Gastric Cancer Patients With Metabolic Syndrome Who Undergo Laparoscopic Radical Gastrectomies: A Polit Randomized Clinical Trial

Qingdao University1 site in 1 country82 target enrollmentSeptember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stomach Neoplasms
Sponsor
Qingdao University
Enrollment
82
Locations
1
Primary Endpoint
The proportion of postoperative complications
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

A prospective randomised controlled trial to investigate the effects of a pre-operative prehabilitation protocol on clinical outcomes of gastric cancer patients with metabolic syndrome who undergo laparoscopic radical gastrectomies and to determine the underlying mechanisms.

Detailed Description

To investigate the effects of a pre-operative prehabilitation protocol on clinical outcomes of gastric cancer patients with metabolic syndrome who undergo laparoscopic radical gastrectomies and to determine the underlying mechanisms.

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
February 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Qingdao University
Responsible Party
Principal Investigator
Principal Investigator

Yanbing Zhou

Professor

Qingdao University

Eligibility Criteria

Inclusion Criteria

  • histologically-proven pre-operative stage I-III gastric cancer
  • Combined with metabolic syndrome
  • Age limits from 18 to 80 years old
  • Classified into American Society of Anesthesiology (ASA) II or III surgical risk
  • no history of abdominal surgery on organs located at the abdominal supramesocolic level

Exclusion Criteria

  • Combined with severe cardiac or pulmonary disease or other organ dysfunction
  • The history of abdominal surgery
  • Conversion to open surgery
  • The presence of gastrointestinal obstruction, perforation or necrosis;
  • Declined to participate in this study

Outcomes

Primary Outcomes

The proportion of postoperative complications

Time Frame: up to six months

Study Sites (1)

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