Effect of Mosapride on Postoperative Ileus in Patients Undergoing Colorectal Surgery (ILEUS)
Postoperative Ileus
About this trial
This is an interventional prevention trial for Postoperative Ileus focused on measuring Postoperative Ileus, Mosapride, Colorectal laparoscopic surgery, Prolonged postoperative ileus
Eligibility Criteria
Inclusion Criteria:
- 18 to 85 years old
- Underwent colonic or upper rectum laparoscopic surgery with diagnose of cancer or malignant polyp
- Were operated on Italian Hospital of Buenos Aires
Exclusion Criteria:
- They refuse to participate from the trial or the process of informed consent
- Have known allergies or hypersensitivity to Mosapride or lactose (used for placebo)
- Patients with ascites, hepatic metastases or carcinomatosis
- Patients who cannot receive Non-steroidal anti-inflammatory drugs
- Pregnancy or women at a fertile age who do not use double contraceptive agents
- Patients with conversion to laparotomy
- Patients with a Rectal tumor beneath 11 cm requiring low or ultralow rectal resection
- Patients with an derivative stoma or who underwent simultaneous resection of other organs
Sites / Locations
- Italian Hospital of Buenos AiresRecruiting
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Active Comparator
Placebo
Mosapride
Placebo arm: intake of placebo (Lactose). 1 pill of the same characteristics as Mosapride every 8 hs with 30 ml tap water. This will begin on postoperative day 1 until discharge from Hospital or unacceptable toxicity develops.
Mosapride arm: intake of active drug (Mosapride). 15 mg per day divided into 3 oral intakes of 5 mg each (1 pill of Mosapride every 8 hs with 30 ml tap water). This treatment will begin on postoperative day 1 until discharge from Hospital or unacceptable toxicity develops.