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Withdrawn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
About this trial
This is an interventional treatment trial for Constipation focused on measuring Intensive care unit, ICU, Critical Illness, Constipation
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
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
NCT ID
NCT02705378
First Posted
February 5, 2016
Last Updated
April 30, 2021
Sponsor
Massachusetts General Hospital
Collaborators
AstraZeneca
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:
PubMed Identifier
16803421
Citation
Patanwala AE, Abarca J, Huckleberry Y, Erstad BL. Pharmacologic management of constipation in the critically ill patient. Pharmacotherapy. 2006 Jul;26(7):896-902. doi: 10.1592/phco.26.7.896.
Results Reference
background
PubMed Identifier
14633751
Citation
Mostafa SM, Bhandari S, Ritchie G, Gratton N, Wenstone R. Constipation and its implications in the critically ill patient. Br J Anaesth. 2003 Dec;91(6):815-9. doi: 10.1093/bja/aeg275.
Results Reference
background
PubMed Identifier
17893628
Citation
van der Spoel JI, Oudemans-van Straaten HM, Kuiper MA, van Roon EN, Zandstra DF, van der Voort PH. Laxation of critically ill patients with lactulose or polyethylene glycol: a two-center randomized, double-blind, placebo-controlled trial. Crit Care Med. 2007 Dec;35(12):2726-31. doi: 10.1097/01.CCM.0000287526.08794.29.
Results Reference
background
PubMed Identifier
19592200
Citation
Nassar AP Jr, da Silva FM, de Cleva R. Constipation in intensive care unit: incidence and risk factors. J Crit Care. 2009 Dec;24(4):630.e9-12. doi: 10.1016/j.jcrc.2009.03.007. Epub 2009 Jul 9.
Results Reference
background
PubMed Identifier
20639749
Citation
Gacouin A, Camus C, Gros A, Isslame S, Marque S, Lavoue S, Chimot L, Donnio PY, Le Tulzo Y. Constipation in long-term ventilated patients: associated factors and impact on intensive care unit outcomes. Crit Care Med. 2010 Oct;38(10):1933-8. doi: 10.1097/CCM.0b013e3181eb9236.
Results Reference
background
PubMed Identifier
16715327
Citation
van der Spoel JI, Schultz MJ, van der Voort PH, de Jonge E. Influence of severity of illness, medication and selective decontamination on defecation. Intensive Care Med. 2006 Jun;32(6):875-80. doi: 10.1007/s00134-006-0175-9. Epub 2006 Apr 28.
Results Reference
background
PubMed Identifier
23370829
Citation
Reintam Blaser A, Poeze M, Malbrain ML, Bjorck M, Oudemans-van Straaten HM, Starkopf J; Gastro-Intestinal Failure Trial Group. Gastrointestinal symptoms during the first week of intensive care are associated with poor outcome: a prospective multicentre study. Intensive Care Med. 2013 May;39(5):899-909. doi: 10.1007/s00134-013-2831-1. Epub 2013 Jan 31.
Results Reference
background
PubMed Identifier
18625051
Citation
Reintam A, Parm P, Kitus R, Starkopf J, Kern H. Gastrointestinal failure score in critically ill patients: a prospective observational study. Crit Care. 2008;12(4):R90. doi: 10.1186/cc6958. Epub 2008 Jul 14. Erratum In: Crit Care. 2008;12(6):435.
Results Reference
background
PubMed Identifier
11837561
Citation
Herndon CM, Jackson KC 2nd, Hallin PA. Management of opioid-induced gastrointestinal effects in patients receiving palliative care. Pharmacotherapy. 2002 Feb;22(2):240-50. doi: 10.1592/phco.22.3.240.33552.
Results Reference
background
PubMed Identifier
20981183
Citation
Masri Y, Abubaker J, Ahmed R. Prophylactic use of laxative for constipation in critically ill patients. Ann Thorac Med. 2010 Oct;5(4):228-31. doi: 10.4103/1817-1737.69113.
Results Reference
background
PubMed Identifier
25303556
Citation
Azevedo RP, Freitas FG, Ferreira EM, Machado FR. Intestinal constipation in intensive care units. Rev Bras Ter Intensiva. 2009 Aug;21(3):324-31. English, Portuguese.
Results Reference
background
PubMed Identifier
22386181
Citation
Sawh SB, Selvaraj IP, Danga A, Cotton AL, Moss J, Patel PB. Use of methylnaltrexone for the treatment of opioid-induced constipation in critical care patients. Mayo Clin Proc. 2012 Mar;87(3):255-9. doi: 10.1016/j.mayocp.2011.11.014.
Results Reference
background
PubMed Identifier
23877147
Citation
Hewitt K, Lin H, Faraklas I, Morris S, Cochran A, Saffle J. Use of methylnaltrexone to induce laxation in acutely injured patients with burns and necrotizing soft-tissue infections. J Burn Care Res. 2014 Mar-Apr;35(2):e106-11. doi: 10.1097/BCR.0b013e31829b399d.
Results Reference
background
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
Learn more about this trial
The Effect of Naloxegol on Refractory Constipation in the Intensive Care Unit
We'll reach out to this number within 24 hrs