The NIPA Study Naloxegol Administration to Prevent Opioids Induced Gastrointestinal Motility Disturbance in Brain Injured PAtients

Brain Injuries Clinical Trial

— NIPA  

Official title:

The NIPA Study: A Randomized Double-blind Control Clinical Trial Naloxegol Administration to Prevent Opioids Induced Gastrointestinal Motility Disturbance in Brain Injured PAtients

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05008926
• Other study ID #: 29BRC18.0262 (NIPA)
• Status: Recruiting
• Phase: Phase 3
• Start date: March 15, 2022
• Est. completion date: September 15, 2026

Study information

• Verified date: January 2024
• Source: University Hospital, Brest
• Contact: Olivier Huet, PU-PH
• Phone: +33 2 98 34 72 88
• Email: olivier.huet[@]chu-brest.fr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Impaired gastrointestinal transit (IGT) especially constipation, is common among patients under mechanical ventilation, occurring in up to 80 % of the patients during the first week, and has been associated with worse outcome in intensive care unit (ICU). Although IGT in critically ill patients is multifactorial and some components are due to complex disease, there is increasing evidence that exogenous opioids contribute to bowel dysmotility. Sedatives and especially opioids are largely used in the brain injured population to control intracranial pression, reduce metabolic rate, manage or prevent seizures, and improve mechanical ventilator synchrony. Therefore, brain injured patients are particularly at risk to develop IGT. The occurrence of IGT is associated with adverse outcomes in intensive care unit. Both gastric reflux and impaired peristaltic contractions are associated with ventilator-acquired pneumonia. The actual challenge is to prevent motility disorders before it occurs. A preventive strategy could in turn reduce the occurrence of complications related to impaired gastrointestinal transit such as ventilator-acquired pneumonia, bacteremia etc. It could also reduce the complications of feed intolerance and thus reduce morbidity and mortality in ICU. Naloxegol is a polyethylene glycol derivative of naloxol, which is a derivative of naloxone and a peripherally acting µ-opioid receptor antagonist. Contrary to naloxone, naloxegol has a very low penetration into the central nervous system, therefore it could be a relevant option for ileus prevention without the risk of impaired sedation. The aim of our study is to assess the efficacy of the administration of naloxegol on the onset of early constipation and early ventilator-acquired pneumonia in brain injured patients receiving opioids for analgosedation.

Description:

Multicenter, randomized, double-blind, placebo-controlled experimental study of Naloxegol.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 370
• Est. completion date: September 15, 2026
• Est. primary completion date: March 22, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Age = to 18 years old

2. Admission to intensive care unit for traumatic brain injury or subarachnoid hemorrhage without other life-threatening injury

3. Patients under sedation with administration of opiate-agonists, µ receptor agonists (Sufentanil, Fentanyl, Remifentanil, Morphine) for less than 24 hours

4. Expected duration of invasive mechanical ventilation and sedation of 48 hours or more

5. Intracranial pressure monitoring

6. Enteral feeding by oro / nasogastric tube

7. Affiliated or beneficiary of the French social security system

Exclusion Criteria:

1. Patient who received opioids for more than 24 hours

2. Patient with refractory intracranial hypertension at the time of inclusion:

intracranial hypertension requiring therapy other than analgo-sedation (thiopental, targeted temperature management, decompressive craniectomy)

3. Acute or chronic renal failure with creatinine clearance <60ml / min

4. Known or suspected acute gastrointestinal obstruction

5. Risk of digestive perforation:

• history of peptic ulcer
• Crohn's disease
• Ogilvie syndrome
• acute diverticulitis
• infiltrating gastrointestinal tumor
• recurrent or advanced ovarian cancer
• peritoneal metastasis
• recent abdominal trauma with risk of digestive perforation

6. Concomitant treatment with a strong or moderate inhibitory effect of CYP 3A4 (For example: clarithromycin, ketaconazole, itraconazole, telithromycin, ritonavir, indinavir, saquinavir) or with a strong inducing effect (carbamazepin, rifampicin, millepertuis)

7. Concomitant treatment with vascular endothelial growth factor (VEGF) inhibitor

8. Allergy to Naloxegol or one of its excipients

9. Recent history of myocardial infarction within the past 6 months, symptomatic congestive cardiovascular disease, QT = 500 msec

10. Patient with a medical decision for rapid palliative care

11. Pregnancy and / or breastfeeding

12. Child Pugh C stage cirrhosis

13. Patient under legal protection or deprived of liberty

14. Patient with another life-threatening injury

15. History of clinically important alterations of the blood-brain barrier: primary brain tumors, metastasis or other inflammatory pathologies in the CNS, active multiple sclerosis, Alzheimer's disease at an advanced stage.

Related Conditions & MeSH terms

• Brain Injuries

Intervention

Drug:
• Naloxegol
Administration of Naloxegol 25 mg per day by nasogastric tube (SNG) or orogastric tube (SOG). The administration should be started within the first 24 hours after the patient is admitted to intensive care and continued for the duration of the administration of the morphine derivative and until 48 hours after its discontinuation.
• Placebo
Administration of the placebo according to the same procedures as the experimental arm.

Locations

Country	Name	City	State
France	CHU Bordeaux	Bordeaux
France	CHU de Bordeaux - Réanimation chirurgicale	Bordeaux
France	CHU Brest	Brest
France	CHU Clermont-Ferrand	Clermont-Ferrand
France	CHU de Montpellier	Montpellier
France	CHU Nantes	Nantes
France	Hôpital La Pitié Salpétrière (APHP)	Paris
France	CHU de Strasbourg	Strasbourg
France	CHU Tours - Hôpital BRETONNEAU	Tours
France	CHU Tours - Hôpital TROUSSEAU	Tours

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of bowel movement		6 days
Primary	Incidence of ventilator-acquired pneumonia		7 days
Secondary	Proportion of patient-days who received the daily calorie goal (25 Kcal / kg / day)		10 days
Secondary	Number of patients who required one or more administration of erythromycin and / or metoclopramide for vomiting occurring during enteral feeding		10 days
Secondary	Number of patients who received one or more rectal laxative for constipation		10 days
Secondary	Time in days of occurrence of the first bowel movement (in case of late constipation)		10 days
Secondary	Number of patients with ventilator-acquired pneumonia after D7 of invasive mechanical ventilationventilation (after D7 of invasive mechanical ventilation)		10 days
Secondary	Number of days without invasive mechanical ventilation		10 days
Secondary	Duration of hospitalization in intensive care unit		10 days
Secondary	Glasgow Outcome Scale Extended Score	The Glasgow Outcome Scale (GOS) is a comprehensive assessment scale for functional outcome that classifies a patient's condition into one of five categories: Death, Vegetative State, Severe Handicap, Moderate Handicap or Good Recovery. The extended GOS scale (GOSE) allows a more detailed classification into eight categories, thanks to a subdivision into two levels (lower and higher) of the categories "severe handicap", "moderate handicap" and "good recovery"	6 month
Secondary	Number of patients who experienced an episode of intracranial hypertension requiring targeted temperature management, barbiturates, or decompression craniectomy.		10 days