Early Alimentation Following Colorectal Surgery
- Conditions
- Colorectal NeoplasmsCrohn Disease
- Registration Number
- NCT00290524
- Lead Sponsor
- Maisonneuve-Rosemont Hospital
- Brief Summary
This study wants to address the question of whether or not oral alimentation should be begun early in patients following colorectal surgery compared to the classical diet which depends on reappearance of functional intestinal transit. Early oral alimentation following colorectal surgery may decrease hospitalisation stay duration.
- Detailed Description
Following intestinal surgery, the classical protocol indicates the use of a naso-gastric tube and starvation more or less prolonged of the patient dependent of surgeon's view. Decision to feed the patient is based on gas and feces reappearance after surgery. However, prolonged starvation might be uncomfortable for the patient as well as increasing his hospitalization stay. Moreover, delayed feeding effect on anastomosis and wound healing is controversial and naso-gastric tube use is known to be uncomfortable and may generate secondary adverse events.
Some studies in opened surgery observed that early alimentation was beneficial against post-surgery mortality, infection risk and anastomosis dehiscence. In addition, early feeding seemed to decrease patient hospitalisation stay.
In order to conduct this study, patients having a colorectal surgery will be randomly attributed to the nil per os group, which is based on the reappearance of a functional intestinal transit, or to the experimental group, which will begin alimentation 12 hours after colorectal surgery.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 800
- Patient 18 years old or more
- Class ASA (American Society of AnaesthesioIogy) 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 or urgent colic resection using laparoscopy or opened surgery defined in section B
Section B: patient must meet one of the following inclusion criterion:
- segmental or total colorectal resection with creation of a primary colo-colic or colo-rectal anastomosis not protected with a derivation ostomy
- ileal resection in continuity with total or a segment of the colon with creation of a primary colo-colic or colo-rectal anastomosis not protected with a derivation ostomy
- Closing of a terminal or loop colostomy
- Class ASA IV or V patient
- Documented problem of gastro-intestinal motility
- Pregnancy
- Any acute or recent (<10 days) septic event
- Chemotherapy during the 4 weeks preceding surgery
- Previous irradiation surrounding the planned anastomosis location
- Small intestine iatrogenic transparietal laceration done during surgery
- Small intestine synchrone resection without continuity with the colon
- Intra-peritoneal chemotherapy administered during or following surgery
- Presence of residual peritoneal carcinosis at the end of surgery
- Colic surgery associated with another major intra-abdominal surgery
- Creation of a colo-anal or ileo-anal anastomosis
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Hospitalisation stay measured in days
- Secondary Outcome Measures
Name Time Method Gastro-intestinal signs and symptoms Treatment of gastro-intestinal signs and symptoms Post-surgery complications
Trial Locations
- Locations (4)
St-Sacrement Hospital
🇨🇦Quebec, Canada
Maisonneuve-Rosemont Hospital
🇨🇦Montreal, Quebec, Canada
St-Luc Hospital
🇨🇦Montreal, Quebec, Canada
Ste-Marie Hospital
🇨🇦Trois-Rivieres, Quebec, Canada