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Trial of Low Residue Diet Versus Clear Liquids Following Elective Colorectal Surgery

Primary Purpose

Nausea/Vomiting

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Clear Liquids
Regular Solid
Abstats
Sponsored by
Cedars-Sinai Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nausea/Vomiting focused on measuring Tolerability diet after surgery

Eligibility Criteria

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

Inclusion Criteria:

  1. Able to freely give written informed consent to participate in the study and have signed the Informed Consent Form;
  2. Males or females, >18 years of age inclusive at the time of study screening;
  3. American Society of Anesthesiologists (ASA) Class I-III;
  4. Colorectal surgery (open and/or robotic/laparoscopic);
  5. Elective Surgery

Exclusion Criteria:

  1. Mentally incompetent or unable or unwilling to provide informed consent or comply with study procedures.
  2. Children <18 years of age.
  3. Pre-operative clinical diagnosis of intestinal obstruction.
  4. Pre-existing known upper gastrointestinal disorders including hiatus hernia, gastroesophageal reflux disease, peptic ulcer disease.
  5. Pre-existing oropharyngeal disorders such as stomatitis, altered taste sensations.
  6. Colorectal surgery with concomitant resectional surgery of the stomach or proximal jejunum (small bowel).
  7. Pregnant patients.
  8. Bedbound or moribund patients.
  9. Pre-existing history of clinical depression.
  10. Epidural analgesia.
  11. Surgical procedures completed after 4pm
  12. Patients taking narcotics prior to elective colorectal surgery

Exclusion Criteria After randomization:

  1. Postoperative diagnosis of intra-abdominal sepsis, including anastomotic leaks.
  2. Postoperative complications requiring early reoperation within the same hospital stay.

Sites / Locations

  • Cedars Sinai Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Clear Liquid Diet

Regular Solid Diet

Arm Description

Clear liquids on postoperative day zero and intestinal rate measured by Abstats

Regular diet from postoperative day zero and intestinal rate measured by Abstats

Outcomes

Primary Outcome Measures

Number of Participants Who Experienced Emesis on Post Operative Day 2
Patient tolerability, as evidenced by development of vomiting on postoperative day two.

Secondary Outcome Measures

Number of Participants Able to Tolerate a Regular Diet as Compared to a Clear Liquid Diet on Post Operative Day 0 (POD 0).
Tolerability of regular diet will be determined by the patients ability to eat more than 50% of a solid meal on post operative day zero.
Antiemetic Usage
If antiemetics were used in
Hospital Stay
Length of postoperative stay
Post-operative Ileus
Development of post-operative ileus
Pain Score
Instrument title: Quality of Life Assessment Visual Analogue scale.Higher scores mean a worse outcome. Pain score evaluated POD 1 and POD 2 and Discharge by using a self reported quality of life measure at regular intervals using a visual analog scale (0-10). A higher score means worse outcome and lower score means better outcome.
Nausea Score
Instrument title: Quality of Life Assessment Visual Analogue scale.Higher scores mean a worse outcome. Nausea Score on POD 1 and POD 2 and Discharge by using a self reported quality of life measure at regular intervals using a visual analog scale (0-10). A higher score means worse outcome and lower score means better outcome.
Bloating Score
Instrument title: Quality of Life Assessment Visual Analogue scale.Higher scores mean a worse outcome. Bloating Score on POD 1 and POD 2 and Discharge by using a self reported quality of life measure at regular intervals using a visual analog scale (0-10). A higher score means worse outcome and lower score means better outcome.

Full Information

First Posted
August 18, 2017
Last Updated
January 17, 2020
Sponsor
Cedars-Sinai Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03260426
Brief Title
Trial of Low Residue Diet Versus Clear Liquids Following Elective Colorectal Surgery
Official Title
Prospective Randomized Controlled Trial Investigating Commencement of Low Residue Diet Versus Clear Liquids on Postoperative Zero Following Elective Colorectal Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
August 16, 2017 (Actual)
Primary Completion Date
July 31, 2018 (Actual)
Study Completion Date
July 31, 2018 (Actual)

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
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Prospective randomized controlled trial investigating commencement of low residue diet versus clear liquids on postoperative zero following elective colorectal surgery, with regards to patient tolerability, incidence of nausea and/or vomiting, and postoperative length of hospitalization stay.
Detailed Description
Offering patients, a low residue diet on the first postoperative day (POD1) after colorectal surgery is safe and improves surgical outcomes and postoperative hospital stay. Early use of low solid is superior to clear liquid diet after elective colorectal surgery. The purpose of this study is to prospectively evaluate whether providing a patient a solid diet from postoperative day zero is superior to clear liquids. The primary endpoint measured will be patient tolerability, as evidenced by absence of vomiting. The secondary endpoints measured will be duration of supplemental intravenous hydration needed, length of hospital stay and postoperative complications, and intestinal rate measured by Abstats. Abstats™ consists of a disposable plastic device embedded with a microphone that adheres to the abdominal wall and connects to a computer measuring acoustic event rates. The monitor will be placed on the patient's abdomen 30 minutes prior to surgery in the preoperative holding area to obtain baseline intestinal rate. The monitor will be removed prior to surgery and replaced by the surgical team in the operating room and maintained until postoperative day 3. Daily intestinal rate will be calculated as mean and median acoustic events per minute. The raw data will be analyzed by an investigator blinded to the clinical data. Intestinal rates of patients offered immediate solid feeds will be compared with those offered clear feeds. In addition, patients not tolerating or consuming early solid meal will be compared with those who do to identify whether Abstat™ can be an early predictor of diet intolerance in patients undergoing colorectal surgery. Patients will be assigned into one of two groups: Group I - Clear liquids on postoperative day zero immediately upon return to the floor and subsequent days' advancement of enteral diet to regular diet is as per discretion of the attending physician. Group II - Regular diet from postoperative day zero immediately upon return to floor and onwards. Three questionnaires assessing quality of life are to be completed by the patient, during his/her hospital stay. On postoperative day one, a self-administered questionnaire is to be completed by the patient. Please see appendix A for the questionnaire details. The same questionnaire is administered on postoperative day two and again on the last day of hospitalization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nausea/Vomiting
Keywords
Tolerability diet after surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Clear Liquid Diet
Arm Type
Experimental
Arm Description
Clear liquids on postoperative day zero and intestinal rate measured by Abstats
Arm Title
Regular Solid Diet
Arm Type
Experimental
Arm Description
Regular diet from postoperative day zero and intestinal rate measured by Abstats
Intervention Type
Dietary Supplement
Intervention Name(s)
Clear Liquids
Intervention Description
Clear liquids on postoperative day zero immediately upon return to the floor and subsequent days' advancement of enteral diet to regular diet is as per discretion of the attending physician.
Intervention Type
Dietary Supplement
Intervention Name(s)
Regular Solid
Intervention Description
Regular diet from postoperative day zero immediately upon return to floor and onwards
Intervention Type
Device
Intervention Name(s)
Abstats
Intervention Description
Intestinal rate measured by Abstats™ in patients offered immediate solid versus clear liquids after colorectal surgery
Primary Outcome Measure Information:
Title
Number of Participants Who Experienced Emesis on Post Operative Day 2
Description
Patient tolerability, as evidenced by development of vomiting on postoperative day two.
Time Frame
POD 2
Secondary Outcome Measure Information:
Title
Number of Participants Able to Tolerate a Regular Diet as Compared to a Clear Liquid Diet on Post Operative Day 0 (POD 0).
Description
Tolerability of regular diet will be determined by the patients ability to eat more than 50% of a solid meal on post operative day zero.
Time Frame
POD 0
Title
Antiemetic Usage
Description
If antiemetics were used in
Time Frame
30 days
Title
Hospital Stay
Description
Length of postoperative stay
Time Frame
30 days
Title
Post-operative Ileus
Description
Development of post-operative ileus
Time Frame
30 days
Title
Pain Score
Description
Instrument title: Quality of Life Assessment Visual Analogue scale.Higher scores mean a worse outcome. Pain score evaluated POD 1 and POD 2 and Discharge by using a self reported quality of life measure at regular intervals using a visual analog scale (0-10). A higher score means worse outcome and lower score means better outcome.
Time Frame
POD 1 and POD 2 and Discharge
Title
Nausea Score
Description
Instrument title: Quality of Life Assessment Visual Analogue scale.Higher scores mean a worse outcome. Nausea Score on POD 1 and POD 2 and Discharge by using a self reported quality of life measure at regular intervals using a visual analog scale (0-10). A higher score means worse outcome and lower score means better outcome.
Time Frame
POD 1 and POD 2 and Discharge
Title
Bloating Score
Description
Instrument title: Quality of Life Assessment Visual Analogue scale.Higher scores mean a worse outcome. Bloating Score on POD 1 and POD 2 and Discharge by using a self reported quality of life measure at regular intervals using a visual analog scale (0-10). A higher score means worse outcome and lower score means better outcome.
Time Frame
POD 1 and POD 2 and Discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Able to freely give written informed consent to participate in the study and have signed the Informed Consent Form; Males or females, >18 years of age inclusive at the time of study screening; American Society of Anesthesiologists (ASA) Class I-III; Colorectal surgery (open and/or robotic/laparoscopic); Elective Surgery Exclusion Criteria: Mentally incompetent or unable or unwilling to provide informed consent or comply with study procedures. Children <18 years of age. Pre-operative clinical diagnosis of intestinal obstruction. Pre-existing known upper gastrointestinal disorders including hiatus hernia, gastroesophageal reflux disease, peptic ulcer disease. Pre-existing oropharyngeal disorders such as stomatitis, altered taste sensations. Colorectal surgery with concomitant resectional surgery of the stomach or proximal jejunum (small bowel). Pregnant patients. Bedbound or moribund patients. Pre-existing history of clinical depression. Epidural analgesia. Surgical procedures completed after 4pm Patients taking narcotics prior to elective colorectal surgery Exclusion Criteria After randomization: Postoperative diagnosis of intra-abdominal sepsis, including anastomotic leaks. Postoperative complications requiring early reoperation within the same hospital stay.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Phillip Fleshner, 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

12. IPD Sharing Statement

Citations:
PubMed Identifier
25203881
Citation
Lau C, Phillips E, Bresee C, Fleshner P. Early use of low residue diet is superior to clear liquid diet after elective colorectal surgery: a randomized controlled trial. Ann Surg. 2014 Oct;260(4):641-7; discussion 647-9. doi: 10.1097/SLA.0000000000000929.
Results Reference
background
PubMed Identifier
25091837
Citation
Spiegel BM, Kaneshiro M, Russell MM, Lin A, Patel A, Tashjian VC, Zegarski V, Singh D, Cohen SE, Reid MW, Whitman CB, Talley J, Martinez BM, Kaiser W. Validation of an acoustic gastrointestinal surveillance biosensor for postoperative ileus. J Gastrointest Surg. 2014 Oct;18(10):1795-803. doi: 10.1007/s11605-014-2597-y. Epub 2014 Aug 5.
Results Reference
background

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Trial of Low Residue Diet Versus Clear Liquids Following Elective Colorectal Surgery

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