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Effect of Mosapride on Postoperative Ileus in Patients Undergoing Colorectal Surgery (ILEUS)

Primary Purpose

Postoperative Ileus

Status
Unknown status
Phase
Phase 4
Locations
Argentina
Study Type
Interventional
Intervention
Mosapride
Placebo
Sponsored by
Hospital Italiano de Buenos Aires
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

Mosapride

Arm Description

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.

Outcomes

Primary Outcome Measures

Number of days after Surgery until the recovery of bowel movement
Effect of the administration of mosapride on the immediate postoperative on the recovery of bowel movements.

Secondary Outcome Measures

Number of patients to develop adverse reactions to Mosapride
To evaluate the safety of the administration of Mosapride after colorectal laparoscopic surgery.

Full Information

First Posted
January 31, 2014
Last Updated
December 16, 2015
Sponsor
Hospital Italiano de Buenos Aires
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1. Study Identification

Unique Protocol Identification Number
NCT02056405
Brief Title
Effect of Mosapride on Postoperative Ileus in Patients Undergoing Colorectal Surgery
Acronym
ILEUS
Official Title
Effect of Mosapride on Postoperative Ileus in Patients Undergoing Colorectal Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Unknown status
Study Start Date
December 2015 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Italiano de Buenos Aires

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Postoperative Ileus is defined as the transient postoperative functional inhibition of propulsive bowel activity. The ethiology of this process can best be described as multifactorial. In its pathogenesis different mechanisms are involved such as hormones and neuropeptides, inflammation, narcotics and the Autonomic nervous system. Is one of the most common causes of prolonged hospital stays after abdominal surgery, thereby increasing health-care resource utilization. More importantly, it causes patient discomfort in the form of nausea, vomiting, and stomach cramps. It has a variable duration but is usually solved in 3 to 4 days. Prolonged Ileus is associated with postoperative complications like an increase on urinary and pulmonary infections, profound venous thrombosis and wound-site complications. Mosapride is a prokinetic agent that acts as a selective serotonin agonist (5- HT4) that facilitates acetylcholine release from the intrinsic plexus. This accelerates gastric emptying and propulsive peristaltic movements on the lower intestines. Mosapride has no action over the central nervous system therefore the lesser side effects like cardiac arrhythmias and extrapyramidal symptoms. For being a safer drug we chose it to be the center of our research. Two randomized controlled trials studied Mosapride concluding it shortens PI after colorectal surgery. However these trials took place on specific populations (Orientals) with less than 50 patients and only one of them included laparoscopic treatment specifically. Also the end point of these studies didn't consider the impact of PI over hospital stay or costs to the health system. We therefore decided to conduct a prospective randomized study in patients undergoing laparoscopic colorectal surgery for colon cancer. The patients will be randomized to receive treatment or placebo after surgery. With this study we intend to prove that patients treated with mosapride immediately after surgery suffer from shorter postoperative ileus with earlier oral intake and shorter hospital stay. The primary aim of the trial is to assess the effectiveness of the use of Mosapride in shortening the duration of the Postoperative ileus in patients undergoing colorectal laparoscopic surgery. The trial hypothesis is that the standardized use of Mosapride immediately after colorectal laparoscopic surgery is safe and accelerates the recovery of propulsive bowel activity, thereby shortening postoperative ileus and hospital stay.
Detailed Description
Methods. Design. Design A randomized controlled trial, triple blind with placebo. Study population Patients undergoing laparoscopic colorectal surgery. Italian Hospital of Buenos Aires. Argentina. Inclusion and exclusion criteria Participants will be eligible provided they are at least 18 years of age and under 85, are about to undergo colonic or upper rectum surgery with the diagnose of cancer o malignant polyp. People will be excluded if: 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 stoma or who underwent simultaneous resection of other organs

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Ileus
Keywords
Postoperative Ileus, Mosapride, Colorectal laparoscopic surgery, Prolonged postoperative ileus

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
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.
Arm Title
Mosapride
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Drug
Intervention Name(s)
Mosapride
Other Intervention Name(s)
Mosar
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Lactose
Intervention Description
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.
Primary Outcome Measure Information:
Title
Number of days after Surgery until the recovery of bowel movement
Description
Effect of the administration of mosapride on the immediate postoperative on the recovery of bowel movements.
Time Frame
1 to 5 days after surgery
Secondary Outcome Measure Information:
Title
Number of patients to develop adverse reactions to Mosapride
Description
To evaluate the safety of the administration of Mosapride after colorectal laparoscopic surgery.
Time Frame
1 to 5 days after surgery
Other Pre-specified Outcome Measures:
Title
Number of days of Hospital stay after surgery.
Description
To assess the effect of Mosapride on the reduction of Hospital stay days
Time Frame
18 months (end of protocol)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Virginia M Cano Busnelli, MD
Phone
54 11 66128852
Email
virginia.cano@hospitalitaliano.org.ar
First Name & Middle Initial & Last Name or Official Title & Degree
Natalia L Gomez, MD
Phone
54 11 68364732
Email
natalia.gomez@hospitalitaliano.org.ar
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carlos A Vaccaro, MD
Organizational Affiliation
Hospital Italiano de Buenos Aires
Official's Role
Study Director
Facility Information:
Facility Name
Italian Hospital of Buenos Aires
City
Buenos Aires
State/Province
State Capital
ZIP/Postal Code
1199
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Virginia M Cano Busnelli, MD
First Name & Middle Initial & Last Name & Degree
Natalia L Gomez, MD
First Name & Middle Initial & Last Name & Degree
Jeremias Goransky Patiño, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
21607794
Citation
Toyomasu Y, Mochiki E, Morita H, Ogawa A, Yanai M, Ohno T, Fujii T, Tsutsumi S, Asao T, Kuwano H. Mosapride citrate improves postoperative ileus of patients with colectomy. J Gastrointest Surg. 2011 Aug;15(8):1361-7. doi: 10.1007/s11605-011-1567-x. Epub 2011 May 24.
Results Reference
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PubMed Identifier
18584249
Citation
Narita K, Tsunoda A, Takenaka K, Watanabe M, Nakao K, Kusano M. Effect of mosapride on recovery of intestinal motility after hand-assisted laparoscopic colectomy for carcinoma. Dis Colon Rectum. 2008 Nov;51(11):1692-5. doi: 10.1007/s10350-008-9407-0. Epub 2008 Jun 27.
Results Reference
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PubMed Identifier
11601663
Citation
Seta ML, Kale-Pradhan PB. Efficacy of metoclopramide in postoperative ileus after exploratory laparotomy. Pharmacotherapy. 2001 Oct;21(10):1181-6. doi: 10.1592/phco.21.15.1181.33888.
Results Reference
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PubMed Identifier
582360
Citation
Davidson ED, Hersh T, Brinner RA, Barnett SM, Boyle LP. The effects of metoclopramide on postoperative ileus. A randomized double-blind study. Ann Surg. 1979 Jul;190(1):27-30. doi: 10.1097/00000658-197907000-00006.
Results Reference
background
PubMed Identifier
4365867
Citation
Furness JB, Costa M. Adynamic ileus, its pathogenesis and treatment. Med Biol. 1974 Apr;52(2):82-9. No abstract available.
Results Reference
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PubMed Identifier
3516299
Citation
Jepsen S, Klaerke A, Nielsen PH, Simonsen O. Negative effect of Metoclopramide in postoperative adynamic ileus. A prospective, randomized, double blind study. Br J Surg. 1986 Apr;73(4):290-1. doi: 10.1002/bjs.1800730414.
Results Reference
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PubMed Identifier
1871540
Citation
Tollesson PO, Cassuto J, Rimback G, Faxen A, Bergman L, Mattsson E. Treatment of postoperative paralytic ileus with cisapride. Scand J Gastroenterol. 1991 May;26(5):477-82. doi: 10.3109/00365529108998569.
Results Reference
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PubMed Identifier
10365879
Citation
Brown TA, McDonald J, Williard W. A prospective, randomized, double-blinded, placebo-controlled trial of cisapride after colorectal surgery. Am J Surg. 1999 May;177(5):399-401. doi: 10.1016/s0002-9610(99)00071-9.
Results Reference
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Effect of Mosapride on Postoperative Ileus in Patients Undergoing Colorectal Surgery

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