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Fast-track Rehabilitation After Elective Colorectal and Small Bowel Resection

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Seoul National University

Status

Completed

Conditions

Colorectal Tumor

Treatments

Behavioral: fast-track rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT00606944
SNUBH-GS-CR1
B-0706-046-008

Details and patient eligibility

About

The purpose of this study is to address the question of whether or not oral alimentation and ambulation exercise should be begun early in patients following laparoscopic colorectal surgery compared to the classical diet and ambulation which depends on reappearance of functional intestinal transit. Early oral alimentation following laparoscopic colorectal surgery may decrease hospital stay and facilitate earlier discharge with comparable postoperative morbidity.

Full description

Traditionally, patients who received laparoscopic colorectal surgery were treated with the classical protocol including the use of a naso-gastric tube and starvation for several postoperative days till the recovery of bowel movement, or bed resting at immediate postoperative period followed by ward ambulation at the postoperative day 1 or 2. Restarting the oral alimentation is based on gas or feces reappearance after surgery and usually this is possible at several days following surgery. However, prolonged starvation might be uncomfortable for the patient as well as increasing his postoperative hospital stay. Recently, several studies reported the efficacy of early rehabilitation protocols after intestinal surgery, showing that early oral alimentation could reduce the length of hospital stay and cost of hospitalization without significant increase of postoperative complications, compared to traditional management.

This prospective, randomized study was designed to evaluate the effectiveness of a postoperative care pathway using rehabilitation with early ambulation and diet for patients undergoing elective laparoscopic colorectal resection compared with the traditional postoperative care.

In order to conduct this study, patients having a laparoscopic colon resection will be randomly attributed to enhanced recovery program group or control group, which is divided based on the postoperative management protocol.

Enrollment

200 patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • • Patients between 20 - 80 years old

    • Class ASA (American Society of Anesthesiology) I, II or III, +/- E
    • Patient willing to participate in the study
    • Patient who understands and accepts to sign the informed consent form
    • Patient who will undergo elective colorectal resection using laparoscopic surgery defined as follows: patients who received one of the following surgery:right hemicolectomy, left hemicolectomy, anterior resection with primary anastomosis, and low anterior resection with loop ileostomy for fecal diversion

Exclusion criteria

  • • Class ASA IV or V patient

    • Documented problem of gastro-intestinal motility
    • Combined resection of other organ than the colorectum
    • Presence of obstructive colorectal cancer associated with dilatation of the proximal gastrointestinal tract
    • Presence of residual peritoneal carcinosis at the end of surgery
    • Previous history of intra-abdominal surgery except simple appendectomy, cholecystectomy, or hysterectomy for uterine myoma
    • Creation of colo-rectal, colo-anal or ileo-anal anastomosis without loop ileostomy
    • Any per-surgery discovery which requires the use of a gastric drainage procedure following surgery
    • Any post-surgery change in patient condition which requires naso-gastric tube holding after surgery

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

ERP group
Experimental group
Description:
fast-track rehabilitation with early ambulation and diet after elective colorectal resection
Treatment:
Behavioral: fast-track rehabilitation
control group
No Intervention group
Description:
traditional, conventional care group

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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