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Intermountain Healthcare's Enhanced Recovery Protocol for Colon Surgery With and Without Alvimopan Use

Primary Purpose

Ileus

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Alvimopam
300 mg Polyethylene
Sponsored by
Intermountain Health Care, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ileus focused on measuring Ileus, Post operative ileus

Eligibility Criteria

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

Inclusion Criteria:

  1. Age > 18
  2. Patient scheduled to receive opioid-based postoperative pain management ≥ 48 hrs
  3. Elective colon/rectal resection with anastomosis as primary procedure
  4. Patient enrolled in multidisciplinary colon care process

Exclusion Criteria:

  1. Pregnancy or lactation
  2. Chronic opioid use or > 3 doses in 7 days prior to surgery
  3. History of multiple previous abdominal operations, gastrectomy, bariatric surgery, short bowel syndrome
  4. Complete bowel obstruction
  5. Patients with end-stage renal disease as defined by the need for dialysis and the commonly accepted threshold for dialysis is a Glomerular Filtration Rate of < 15.
  6. Patients with severe hepatic impairment (Childs-Pugh class C)
  7. ASA 4 or 5 (ASA 4 s incapacitating systemic disease that is a constant threat to life)
  8. Non-English speaking patients

Sites / Locations

  • American Fork Hospital
  • Valley View Hospital
  • Logan Regional Hospital
  • Intermoutain Medical Center
  • McKay-Dee Hospital
  • Utah Valley
  • LDS Hospital
  • Alta View Hospital
  • Dixie Regional

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

300 mg Polyethylene

Alvimopan

Arm Description

Outcomes

Primary Outcome Measures

Measure of Improvement Over the Standard
Determine if alvimopan addition to the multidisciplinary care process will result in decreased length of stay compared with the multidisciplinary care process plus placebo. Length of stay is determined by how many days a patient stays in the hospital. This is calculated by subtracting the discharge date from the admit date.

Secondary Outcome Measures

Hospital Cost
Total Cost of hospital stay inflation adjusted to 2010 dollars.

Full Information

First Posted
May 24, 2010
Last Updated
August 25, 2014
Sponsor
Intermountain Health Care, Inc.
Collaborators
Cubist Pharmaceuticals LLC
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1. Study Identification

Unique Protocol Identification Number
NCT01143259
Brief Title
Intermountain Healthcare's Enhanced Recovery Protocol for Colon Surgery With and Without Alvimopan Use
Official Title
A Randomized, Double Blind, Placebo Controlled Study to Study Intermountain Healthcare's Enhanced Recovery Protocol for Colon Surgery With and Without Alvimopan Use
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
August 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Intermountain Health Care, Inc.
Collaborators
Cubist Pharmaceuticals LLC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine if the addition of alvimopan to our care process model for colon resection patients will decrease length of stay. The care process model is a combination of optimal IV fluid management, early feeding, early ambulation, patient education, and pain management.
Detailed Description
Narcotic pain medicines bind mu-opioid receptors in the bowel and delay the return of normal function. Alvimopan is a peripherally acting mu-opioid receptor antagonist that blocks mu-opioid receptors in the gastrointestinal tract but does not compromise central nervous system-mediated opioid-based analgesia. Length of stay is an important surrogate measure of quality after colon surgery and the most common reason for prolonged Length of Stay after abdominal surgery is delayed gastrointestinal recovery (postoperative ileus). The Food and Drug Administration has approved alvimopan (dosed preoperatively and twice daily postoperatively for up to 15 in-hospital doses) for the acceleration of upper and lower gastrointestinal recovery after partial bowel resection with primary anastomosis. In the 5 phase III alvimopan efficacy trials, a simple standardized accelerated postoperative care pathway was used rather than a comprehensive, multidisciplinary colon surgery care process model that is used by Intermountain Healthcare. In the most recently completed alvimopan phase III trial, the mean postoperative length of stay was 5.2 days whereas the mean length of stay at Intermountain Healthcare is 4.4 days without the addition of alvimopan to the multidisciplinary colon care process model. This trial will investigate if the addition of alvimopan to the Intermountain Healthcare multidisciplinary care process can decrease length of stay compared with the multidisciplinary care process plus placebo.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ileus
Keywords
Ileus, Post operative ileus

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
274 (Actual)

8. Arms, Groups, and Interventions

Arm Title
300 mg Polyethylene
Arm Type
Placebo Comparator
Arm Title
Alvimopan
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Alvimopam
Other Intervention Name(s)
Entereg
Intervention Description
The treatment group will receive 12mg of Alvimopan by mouth 30 to 90 minutes before surgery and twice daily till discharge or to a maximum of 7 days (15 doses, total) after surgery.12 mg by mouth 30 to 90 minutes before surgery and twice daily till discharge or to a maximum of 7 days.
Intervention Type
Drug
Intervention Name(s)
300 mg Polyethylene
Intervention Description
The control group will receive 300mg of polyethylene glyco by mouth 30 to 90 minutes before surgery and twice daily till discharge or to a maximum of 7 days (15 doses, total) after surgery.
Primary Outcome Measure Information:
Title
Measure of Improvement Over the Standard
Description
Determine if alvimopan addition to the multidisciplinary care process will result in decreased length of stay compared with the multidisciplinary care process plus placebo. Length of stay is determined by how many days a patient stays in the hospital. This is calculated by subtracting the discharge date from the admit date.
Time Frame
Number of days the patient stayed in the hospital [Time frame: Inpatient admit day to discharge day]
Secondary Outcome Measure Information:
Title
Hospital Cost
Description
Total Cost of hospital stay inflation adjusted to 2010 dollars.
Time Frame
Upon discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 Patient scheduled to receive opioid-based postoperative pain management ≥ 48 hrs Elective colon/rectal resection with anastomosis as primary procedure Patient enrolled in multidisciplinary colon care process Exclusion Criteria: Pregnancy or lactation Chronic opioid use or > 3 doses in 7 days prior to surgery History of multiple previous abdominal operations, gastrectomy, bariatric surgery, short bowel syndrome Complete bowel obstruction Patients with end-stage renal disease as defined by the need for dialysis and the commonly accepted threshold for dialysis is a Glomerular Filtration Rate of < 15. Patients with severe hepatic impairment (Childs-Pugh class C) ASA 4 or 5 (ASA 4 s incapacitating systemic disease that is a constant threat to life) Non-English speaking patients
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bob Moesinger, MD
Organizational Affiliation
Intermountain Health Care, Inc.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Matthew Peters, RN
Organizational Affiliation
Intermountain Health Care, Inc.
Official's Role
Study Director
Facility Information:
Facility Name
American Fork Hospital
City
American Fork
State/Province
Utah
ZIP/Postal Code
84003
Country
United States
Facility Name
Valley View Hospital
City
Cedar City
State/Province
Utah
ZIP/Postal Code
84721
Country
United States
Facility Name
Logan Regional Hospital
City
Logan
State/Province
Utah
ZIP/Postal Code
84341
Country
United States
Facility Name
Intermoutain Medical Center
City
Murray
State/Province
Utah
ZIP/Postal Code
84157
Country
United States
Facility Name
McKay-Dee Hospital
City
Ogden
State/Province
Utah
ZIP/Postal Code
84403
Country
United States
Facility Name
Utah Valley
City
Provo
State/Province
Utah
ZIP/Postal Code
84604
Country
United States
Facility Name
LDS Hospital
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84103
Country
United States
Facility Name
Alta View Hospital
City
Sandy
State/Province
Utah
ZIP/Postal Code
84094
Country
United States
Facility Name
Dixie Regional
City
St. George
State/Province
Utah
ZIP/Postal Code
84790
Country
United States

12. IPD Sharing Statement

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Intermountain Healthcare's Enhanced Recovery Protocol for Colon Surgery With and Without Alvimopan Use

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