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Implementing a Low Fiber Diet vs. Regular Diet in Postoperative Colorectal Patients With Ileostomies

Primary Purpose

Ileostomy; Complications, Bowel Obstruction, Postoperative Ileus

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Regular diet
Low fiber diet
Sponsored by
Cedars-Sinai Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Ileostomy; Complications focused on measuring Ileostomy, Bowel obstruction, Postoperative ileus, Low fiber diet, Regular diet

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Male or Female
  2. Undergoing elective or urgent major laparoscopic or open colorectal procedure resulting in new loop or end ileostomy creation
  3. Urgent colorectal surgery is defined as operations performed during the same hospital admission, but greater than 24hrs after decision for surgery is made. Patients undergoing urgent colorectal surgery are not expected to require intensive care unit (ICU) admission postoperatively.
  4. Willingness and ability to sign an informed consent document
  5. No allergies to anesthetic or antiemetic
  6. ASA physical status Class I - III
  7. Aged 18-90 years

Exclusion Criteria:

  1. Refusal to participate in the study
  2. Undergoing emergent colorectal surgery. Emergent colorectal surgery is defined as patients who require immediate surgery < 24hrs after initial decision for surgery is made
  3. Patients expected to require intensive care unit (ICU) admission postoperatively
  4. Age <18 or > 90 years
  5. Pregnancy
  6. Patient with preoperative short-bowel syndrome or proximal stomas (jejunostomy)
  7. Patients on preoperative total parenteral nutrition not expected to immediately commence postoperative enteral nutrition
  8. Patients maintained NPO for any reason after surgery

Sites / Locations

  • Cedars Sinai Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Low fiber diet

Regular diet

Arm Description

Patients in this arm will receive low fiber diet starting postoperative day 1. This is currently the standard protocol at our institution.

Patients in this arm will receive regular diet starting postoperative day 1. This will be the experimental arm.

Outcomes

Primary Outcome Measures

Rate of postoperative ileus and obstruction
evaluate rate of post-operative ileus or obstruction in patients with ileostomies receiving low fiber diet vs. regular diet starting post-operative day 1.

Secondary Outcome Measures

Hospital readmission rates
Hospital readmission rates
Hospital length of stay
Hospital length of stay
Volume of stoma output
Average daily volume of stoma output
Need for antidiarrheal use
Need for antidiarrheal use
Average maximum daily nausea score
Average maximum daily nausea score on a scale of 0 to 2. A score of 0 means no presence of nausea, 1 denotes presence of nausea, and 2 denotes presence of vomiting. A higher score up to a maximum of 2 means a worse outcome compared to a lower score.
Average maximum daily pain score
Average maximum daily pain score on a scale of 0 to 10. A score of 0 means a patient has no pain. A higher score up to the maximum of 10 means a worse outcome.
Quality of life
Quality of life assessed using the Gastrointestinal Quality of Life Index (GIQLI) questionnaire. The GIQLI questionnaire has 36 items, each item is scored 0 to 4. The GIQLI has a range of 0 to 144. Higher score up to a maximum of 144 means better outcome.

Full Information

First Posted
December 2, 2020
Last Updated
October 20, 2022
Sponsor
Cedars-Sinai Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04675606
Brief Title
Implementing a Low Fiber Diet vs. Regular Diet in Postoperative Colorectal Patients With Ileostomies
Official Title
A Prospective Randomized Trial of Low Fiber Diet vs. Regular Diet in Postoperative Colorectal Patients With Ileostomies
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 21, 2020 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cedars-Sinai Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The primary objective of this study is to prospectively evaluate rate of post-operative ileus or obstruction in patients with ileostomies receiving low fiber diet vs. regular diet starting post-operative day 1. The secondary objectives of this study are to compare the 30-day and 90-day readmission rates, length of stay, rate of high stoma output or need for antidiarrheals within 90 days, nausea score, level of pain, and overall quality of life amongst the patients studied.
Detailed Description
The proposed study is a prospective randomized study to compare two post-operative diets Low fiber diet Regular diet in patients undergoing elective or urgent colorectal surgery resulting in a loop or end ileostomy. The primary outcome measure is rate of post-operative ileus or obstruction in patients with ileostomies. The secondary objectives of this study are to compare the length of stay, 30-day and 90-day readmission rates, rate of high stoma output requiring antidiarrheal medication, nausea score, pain score, and overall quality of life amongst the patients studied. All groups will be counseled and asked to consent for the study at the time of their preoperative clinic visit and copy of the protocol will be provided to them. Patients undergoing urgent surgery will be counseled and consented at the time decision for surgery is made. All groups will be started on either low fiber diet or regular diet on postoperative day 1. Of note, it is important to note that at our institution, a "low fiber diet" is equivalent to a "low residue diet" in our electronic medical records system. All groups will be assessed and examined daily, where nausea score and pain score will be recorded. Prior to discharge, both groups will receive consultation with a wound-ostomy care nurse who will perform ostomy teaching as well as diet/nutritional counseling. Patients in the low fiber diet arm will receive nutritional counseling advising that they follow a low fiber diet. Patients in the regular diet arm will receive nutritional counseling advising that they continue to follow a regular diet.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ileostomy; Complications, Bowel Obstruction, Postoperative Ileus
Keywords
Ileostomy, Bowel obstruction, Postoperative ileus, Low fiber diet, Regular diet

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
160 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Low fiber diet
Arm Type
Active Comparator
Arm Description
Patients in this arm will receive low fiber diet starting postoperative day 1. This is currently the standard protocol at our institution.
Arm Title
Regular diet
Arm Type
Experimental
Arm Description
Patients in this arm will receive regular diet starting postoperative day 1. This will be the experimental arm.
Intervention Type
Behavioral
Intervention Name(s)
Regular diet
Intervention Description
Patients in the regular diet arm (which is the experimental arm) will not have any diet limitations and will be recommended to consume a healthy balanced diet for American adults as recommended by the United States Department of Agriculture (USDA) and US Food and Drug Administration (FDA).
Intervention Type
Behavioral
Intervention Name(s)
Low fiber diet
Other Intervention Name(s)
Low residue diet
Intervention Description
Patients in the low fiber diet arm (which is the control arm) will be recommended to consume foods that are low in fiber content per United Ostomy Associations of America Recommendations
Primary Outcome Measure Information:
Title
Rate of postoperative ileus and obstruction
Description
evaluate rate of post-operative ileus or obstruction in patients with ileostomies receiving low fiber diet vs. regular diet starting post-operative day 1.
Time Frame
90 days postoperatively
Secondary Outcome Measure Information:
Title
Hospital readmission rates
Description
Hospital readmission rates
Time Frame
90 days postoperatively
Title
Hospital length of stay
Description
Hospital length of stay
Time Frame
Up to 90 days postoperatively
Title
Volume of stoma output
Description
Average daily volume of stoma output
Time Frame
90 days postoperatively
Title
Need for antidiarrheal use
Description
Need for antidiarrheal use
Time Frame
90 days postoperatively
Title
Average maximum daily nausea score
Description
Average maximum daily nausea score on a scale of 0 to 2. A score of 0 means no presence of nausea, 1 denotes presence of nausea, and 2 denotes presence of vomiting. A higher score up to a maximum of 2 means a worse outcome compared to a lower score.
Time Frame
90 days postoperatively
Title
Average maximum daily pain score
Description
Average maximum daily pain score on a scale of 0 to 10. A score of 0 means a patient has no pain. A higher score up to the maximum of 10 means a worse outcome.
Time Frame
90 days postoperatively
Title
Quality of life
Description
Quality of life assessed using the Gastrointestinal Quality of Life Index (GIQLI) questionnaire. The GIQLI questionnaire has 36 items, each item is scored 0 to 4. The GIQLI has a range of 0 to 144. Higher score up to a maximum of 144 means better outcome.
Time Frame
90 days postoperatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male or Female Undergoing elective or urgent major laparoscopic or open colorectal procedure resulting in new loop or end ileostomy creation Urgent colorectal surgery is defined as operations performed during the same hospital admission, but greater than 24hrs after decision for surgery is made. Patients undergoing urgent colorectal surgery are not expected to require intensive care unit (ICU) admission postoperatively. Willingness and ability to sign an informed consent document No allergies to anesthetic or antiemetic ASA physical status Class I - III Aged 18-90 years Exclusion Criteria: Refusal to participate in the study Undergoing emergent colorectal surgery. Emergent colorectal surgery is defined as patients who require immediate surgery < 24hrs after initial decision for surgery is made Patients expected to require intensive care unit (ICU) admission postoperatively Age <18 or > 90 years Pregnancy Patient with preoperative short-bowel syndrome or proximal stomas (jejunostomy) Patients on preoperative total parenteral nutrition not expected to immediately commence postoperative enteral nutrition Patients maintained NPO for any reason after surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lucille Yao, MD
Phone
310-289-9224
Email
lucille.yao@cshs.org
First Name & Middle Initial & Last Name or Official Title & Degree
Karen Zaghiyan, MD
Phone
310-289-9224
Email
karen.zaghiyan@cshs.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karen Zaghiyan, MD
Organizational Affiliation
Cedars-Sinai Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cedars Sinai Medical Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90048
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lucille Yao, MD
Phone
310-289-9224
Email
lucille.yao@cshs.org
First Name & Middle Initial & Last Name & Degree
Karen Zaghiyan, MD
Phone
310-289-9224
Email
karen.zaghiyan@cshs.org
First Name & Middle Initial & Last Name & Degree
Phillip Fleshner, MD
First Name & Middle Initial & Last Name & Degree
Karen Zaghiyan, MD
First Name & Middle Initial & Last Name & Degree
Lucille Yao, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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Results Reference
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Results Reference
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Links:
URL
https://www.sealedenvelope.com/power/binary-noninferior/
Description
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Implementing a Low Fiber Diet vs. Regular Diet in Postoperative Colorectal Patients With Ileostomies

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