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The Effect of Naloxegol on Refractory Constipation in the Intensive Care Unit (NaRC-ICU)

Primary Purpose

Constipation, Critical Illness

Status
Withdrawn
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Polyethylene glycol
naloxegol
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Constipation focused on measuring Intensive care unit, ICU, Critical Illness, Constipation

Eligibility Criteria

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

Inclusion Criteria:

  1. Age ≥18 years
  2. Admitted to an ICU at Massachusetts General Hospital (MGH)
  3. Received ≥72 hours of continuous opioid infusion
  4. Anticipated to require ≥48 hours of additional care in the ICU
  5. Did not have a bowel movement in ≥72 hours
  6. Allowed to receive (and tolerating) medications via nasogastric, orogastric, gastric, gastrojejunal, or oral route
  7. Receiving at least trophic (10 mL/hr) of enteral nutrition

Exclusion Criteria:

  1. Unable to provide informed consent or unavailable healthcare proxy
  2. Not expected to survive >48 hours from time of enrollment
  3. "Comfort measures only" status (i.e. palliative care)
  4. Received medication other that docusate and senna glycoside for laxation
  5. Had abdominal surgery that is expected to cause significant ileus
  6. Mechanical bowel obstruction
  7. Total bowel rest/exclusively receiving total parenteral nutrition
  8. History of chronic constipation unrelated to opioid use
  9. Compromised blood-brain-barrier
  10. Current diagnosis of solid organ or hematologic cancer
  11. On moderate/strong CYP3A4 inhibitors or strong CYP3A4 inducers
  12. On other opioid antagonists
  13. Pregnant or lactating females

Sites / Locations

  • Massachusetts General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Polyethylene glycol

naloxegol

Arm Description

17g power qday; reconstituted in water for naso/orogastric tube administration

25mg qday; crushed pill reconstituted in water for naso/orogastric tube administration

Outcomes

Primary Outcome Measures

Laxation within 48 hours of starting second-line agent
Documented bowel movement (Yes/No) within 48 hours of randomization to receive second-line laxative agent

Secondary Outcome Measures

Time to first bowel movement after starting second-line agent
Number of hours from initiation of a second-line laxative agent until first documented bowel movement
Doses of second-line laxative agent before bowel movement
Number of doses of second-line laxative agent until first documented bowel movement
Protein/caloric deficit
Cumulative calorie and protein deficits will be calculated in kcals and grams, respectively, utilizing standard clinical formulas from the day of ICU admission until day 7 of ICU admission
Feeding interruptions
Number of interruptions to enteral nutrition for high gastric residual volume during study period

Full Information

First Posted
February 5, 2016
Last Updated
April 30, 2021
Sponsor
Massachusetts General Hospital
Collaborators
AstraZeneca
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1. Study Identification

Unique Protocol Identification Number
NCT02705378
Brief Title
The Effect of Naloxegol on Refractory Constipation in the Intensive Care Unit
Acronym
NaRC-ICU
Official Title
The Effect of Naloxegol on Refractory Constipation in the Intensive Care Unit
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Withdrawn
Why Stopped
PI left institution. Protocol never submitted to the IRB, no contract executed only Confidentiality Agreement, and study not done.
Study Start Date
May 2017 (Anticipated)
Primary Completion Date
April 2019 (Anticipated)
Study Completion Date
December 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Massachusetts General Hospital
Collaborators
AstraZeneca

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Naloxegol has recently been approved by the US Food and Drug Administration to treat opioid induced constipation in non-cancer chronic pain patients. Its effectiveness in acute care patients, however, is not known. Therefore, the researchers' goal is to investigate whether naloxegol is superior to osmotic laxatives for refractory constipation in ICU patients already receiving prophylactic stool softeners and simulant laxatives through a double-blind, randomized control trial.
Detailed Description
Constipation is often defined as the absence of a bowel movement for 3 consecutive days. The incidence of constipation in critically ill patients is estimated to be 50-80%. Constipation in the ICU is associated with various undesirable clinical outcomes, including: increased rate of infections, prolonged duration of mechanical ventilation, greater hospital length of stay, worsening of organ dysfunction, and even higher mortality. Typical first-line agents for the management of ICU constipation include stool softeners (e.g. docusate) and bowel stimulants (e.g. senna glycol or bisacodyl), and these are often used prophylactically in critically ill patients. However, a significant proportion of patients require additional therapy to promote laxation , the most common being osmotic agents such as propylene glycol or lactulose. Often, multiple doses of osmotic agents over several days are required to achieve acceptable laxation rates during critical illness. As such, this has prompted the need for targeted therapy to improve constipation in the ICU. Among major risk factors for constipation in the ICU are the lack of bowel stimulation via nutrition and exposure to high doses of continuous opioids . Indeed, clinical data suggests that early enteral nutrition promotes laxation in ICU patients. And recently, methylnaltrexone, a peripherally acting μ-opioid receptor antagonist, has shown promising results in its ability to reverse opioid-induced constipation. However, methylnaltrexone is delivered via subcutaneous injection and its absorption is likely to be variable in critically ill patients who often receive aggressive fluid resuscitation and have significant peripheral edema. The US Food and Drug Administration recently approved the use of naloxegol, a μ-opioid receptor antagonist available in tablet form, for the management of opioid-induced constipation in non-cancer chronic pain patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Constipation, Critical Illness
Keywords
Intensive care unit, ICU, Critical Illness, Constipation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Polyethylene glycol
Arm Type
Active Comparator
Arm Description
17g power qday; reconstituted in water for naso/orogastric tube administration
Arm Title
naloxegol
Arm Type
Experimental
Arm Description
25mg qday; crushed pill reconstituted in water for naso/orogastric tube administration
Intervention Type
Drug
Intervention Name(s)
Polyethylene glycol
Other Intervention Name(s)
Polyethylene glycol (PEG), miralax, glycolax
Intervention Description
Intervention would be given by oro-gastric (OG) or naso-gastric (NG) tube
Intervention Type
Drug
Intervention Name(s)
naloxegol
Other Intervention Name(s)
Movantik
Intervention Description
Intervention would be given by OG or NG tube
Primary Outcome Measure Information:
Title
Laxation within 48 hours of starting second-line agent
Description
Documented bowel movement (Yes/No) within 48 hours of randomization to receive second-line laxative agent
Time Frame
From 72 hours after ICU admission until 120 hours after ICU admission
Secondary Outcome Measure Information:
Title
Time to first bowel movement after starting second-line agent
Description
Number of hours from initiation of a second-line laxative agent until first documented bowel movement
Time Frame
From 72 hours after ICU admission until 120 hours after ICU admission
Title
Doses of second-line laxative agent before bowel movement
Description
Number of doses of second-line laxative agent until first documented bowel movement
Time Frame
From 72 hours after ICU admission until 120 hours after ICU admission
Title
Protein/caloric deficit
Description
Cumulative calorie and protein deficits will be calculated in kcals and grams, respectively, utilizing standard clinical formulas from the day of ICU admission until day 7 of ICU admission
Time Frame
From admission to the ICU until the end of day 7 after ICU admission
Title
Feeding interruptions
Description
Number of interruptions to enteral nutrition for high gastric residual volume during study period
Time Frame
From admission to the ICU until the end of day 7 after ICU admission

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years Admitted to an ICU at Massachusetts General Hospital (MGH) Received ≥72 hours of continuous opioid infusion Anticipated to require ≥48 hours of additional care in the ICU Did not have a bowel movement in ≥72 hours Allowed to receive (and tolerating) medications via nasogastric, orogastric, gastric, gastrojejunal, or oral route Receiving at least trophic (10 mL/hr) of enteral nutrition Exclusion Criteria: Unable to provide informed consent or unavailable healthcare proxy Not expected to survive >48 hours from time of enrollment "Comfort measures only" status (i.e. palliative care) Received medication other that docusate and senna glycoside for laxation Had abdominal surgery that is expected to cause significant ileus Mechanical bowel obstruction Total bowel rest/exclusively receiving total parenteral nutrition History of chronic constipation unrelated to opioid use Compromised blood-brain-barrier Current diagnosis of solid organ or hematologic cancer On moderate/strong CYP3A4 inhibitors or strong CYP3A4 inducers On other opioid antagonists Pregnant or lactating females
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sadeq A. Quraishi, MD,MHA,MMSc
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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16803421
Citation
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Results Reference
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Links:
URL
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642590/
Description
Constipation in critically ill patients and its relationship to feeding and weaning from respiratory support

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The Effect of Naloxegol on Refractory Constipation in the Intensive Care Unit

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