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Fast Track Laparoscopic Surgery: A Better Option for Treating Colorectal Cancer Than Conventional Laparoscopic Surgery

Fast Track Laparoscopic Surgery: A Better Option for Treating Colorectal Cancer Than Conventional Laparoscopic Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01969591
Acronym
FTS
Enrollment
70
Registered
2013-10-25
Start date
2011-01-31
Completion date
2013-09-30
Last updated
2013-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer

Keywords

Fast track surgery, Laparoscopic surgery, colorectal cancer

Brief summary

To compare the outcomes of fast track laparoscopic surgery and conventional laparoscopic surgery.

Detailed description

Method: This study is a blinded randomized trial. 70 patients with colorectal cancer will undergo laparoscopic colorectal resection, and will be divided into two groups. Protocols for fast-track group includes skipping preoperative mechanical bowel preparation, early restoration of diet and early postoperative ambulation. Outcome measures, length of hospital stay, postoperative surgical stress response (C reactive protein) and postoperative complications will be compared between the two groups.

Interventions

Patients with colorectal cancer will undergo laparoscopic colorectal resection, and will be divided into two groups. Protocols for fast-track group includes skipping preoperative mechanical bowel preparation, early restoration of diet and early postoperative ambulation.

OTHERconventional postoperative surgery

Patients with colorectal cancer will undergo laparoscopic colorectal resection, and will be divided into two groups. Protocols for fast-track group includes skipping preoperative mechanical bowel preparation, early restoration of diet and early postoperative ambulation.

Sponsors

Quan Wang
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
No minimum to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age ≤75 years * Good nutrition * no systemic infection * Elective laparoscopic surgery

Exclusion criteria

* Age \>75 years * Malnutrition or an organ system infection * Associated with obstruction, bleeding, emergency surgery or surgical intervention * Tumor with extensive metastasis * Before operation patient was fasting, underwent gastrointestinal decompression and received nutritional support * Previous history of abdominal surgery * Patient had previously undergone gastrostomy

Design outcomes

Primary

MeasureTime frame
solid diet timewith the first 30 days(plus or minus 3days) after surgery
Postoperative dayswith the first 30 days(plus or minus 3days) after surgery
First flatus timewith the first 30 days(plus or minus 3days) after surgery
First defecation timewith the first 30 days(plus or minus 3days) after surgery
Length of hospital staywith the first 30 days(plus or minus 3days) after surgery

Secondary

MeasureTime frame
CRP (mg/L)with the first 30 days(plus or minus 3days) after surgery
Complications:anastomotic leakage,intestinal obstruction,wound infectionone year
Analgesicswith the first 30 days(plus or minus 3days) after surgery

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026