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Effect of Naloxegol on Postoperative Ileus in Patients Undergoing Cardiac Surgery (TRANSIT)

Primary Purpose

Postoperative Ileus (Post Cardiac Surgery Constipation)

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Naloxegol
inert tablet
Sponsored by
CMC Ambroise Paré
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postoperative Ileus (Post Cardiac Surgery Constipation) focused on measuring Opioid induced constipation, cardiac surgery, transit recovery

Eligibility Criteria

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

Inclusion Criteria:

  • > 18 years old,
  • Undergoing cardiac surgery with cardiopulmonary bypass,
  • For women of child bearing potential without contraception, beta-HCG negative result
  • Having signed a written informed consent form,
  • Affiliation to the social security system.

Exclusion Criteria:

  • Allergy or known hypersensitivity to Naloxegol or any of the excipients or any other opioid antagonist
  • Pregnant or breastfeeding women
  • Severe hepatic failure, history of cirrhosis
  • Moderate or severe renal failure (GFR<60ml/min)
  • Concomitant treatment with a strong cytochrome P450 3A4 inhibitor
  • History of acute gastro-intestinal obstruction known or suspected
  • History of digestive arteritis
  • Clinically relevant alteration of the blood-brain-barrier
  • Cancer with increased risk of gastro-duodenal perforation
  • Disorder that could alter the integrity of the gastrointestinal lining
  • Regular treatment with laxative drugs
  • Concomitant treatment with methadone
  • Patient unable to take a drug by oral route
  • Patient under protection of the adults (guardianship, curators or safeguard of justice),
  • Patient included or planning to be included in another research protocol relating to medications.

Sites / Locations

  • CMC Ambroise Paré

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Naloxegol group

Placebo group

Arm Description

naloxégol tablet by oral route

inert tablet by oral route

Outcomes

Primary Outcome Measures

Evaluate the effect of perioperative naloxegol administration on the duration of postoperative ileus after cardiac surgery
Time (hour) to transit recovery after cardiac surgery

Secondary Outcome Measures

Incidence of digestive complications
rate of digestive complications
Evaluate the effect of the administration of Naloxegol on respiratory complications
rate of respiratory complications
Evaluate the effect of the administration of Naloxegol on infectious complications
rate of infectious complications
Verify the effectiveness of analgesia
Pain Visual Analogue Scale (VAS) ranging from 0 to 10 (0=no pain, 10=worst possible pain)
Compare the length of hospital stay
Duration of hospital stay (days)
Compare the length of ICU stay
Duration of ICU stay (days)

Full Information

First Posted
June 12, 2020
Last Updated
March 7, 2022
Sponsor
CMC Ambroise Paré
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1. Study Identification

Unique Protocol Identification Number
NCT04433390
Brief Title
Effect of Naloxegol on Postoperative Ileus in Patients Undergoing Cardiac Surgery
Acronym
TRANSIT
Official Title
Time to Transit Recovery After Treatment With Naloxegol in Cardiac Surgery Intensive Care Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
October 14, 2020 (Actual)
Primary Completion Date
January 28, 2022 (Actual)
Study Completion Date
March 3, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CMC Ambroise Paré

4. Oversight

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

5. Study Description

Brief Summary
Postoperative ileus, defined as the transient postoperative functional inhibition of propulsive bowel activity, commonly occurs in patients after cardiac surgery and contributes to postoperative morbidity. Naloxegol is a peripheral opioid receptor antagonist. Recent studies showed that naloxegol is effective in the treatment of chronic opioid-induced constipation but there is no data on its use in the management of postoperative ileus after cardiac surgery. The main objective of this prospective, double-blind, randomized, placebo-controlled trial is to assess the effectiveness of the perioperative use of naloxegol in reducing the duration of the postoperative ileus in patients undergoing cardiac surgery.
Detailed Description
Digestive complications following cardiac surgery, such as paralytic ileus and Ogilvie syndrome, are frequent and worsen the prognosis of patients. They pose a real problem of care in intensive care, inducing morbidity and mortality, extended hospital stay and a significant post-operative cost. Few treatments are effective to reduce transit recovery time, except the neostigmine which has a serious side effects including cardiac ones. During cardiac surgery, opioid treatments are frequently used to relieve the pain like sternotomy pain. The pharmacologic effect of opioid induces the postoperative uleus. Opioid receptors are distributed in the central nervous system, where they are involved in the perception of pain, and in the peripheral nervous system, especially in the mesenteric nervous system, where they regulate intestinal peristalsis. Morphine receptors antagonist are a target for prevention and treatment of post operative ileus syndrome such as alvimopan and naloxone. A therapeutic trial demonstrates a decrease in the rate of pneumonia in intensive care patient mechanically ventilated who received naloxone. Naloxegol is a peripheral antagonist of opioid receptor, from the alvimopan family. It has been designed to antagonize the peripheral, but not central, effects of opioids at therapeutic doses. Naloxegol is a substrate for cytochrome P450 (CYP 3A4). Following oral administration, naloxegol is absorbed rapidly, with peak concentrations achieved at less than 2 hours. After once daily administration, plasma concentration equilibrium is reached within 2-3 days with minimal accumulation. The main route of elimination for naloxegol is hepatic. Naloxegol has been shown to be effective in randomized trials of chronic opioid induced constipation, but there is no data on its use in the postoperative ileus. Research hypothesis: the addition of naloxegol in pre and postoperative cardiac surgery could reduce the time to transit recovery and the rate of digestive and respiratory complications.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Ileus (Post Cardiac Surgery Constipation)
Keywords
Opioid induced constipation, cardiac surgery, transit recovery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
the nurse giving the treatment is not the outcomes assessor.
Allocation
Randomized
Enrollment
305 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Naloxegol group
Arm Type
Experimental
Arm Description
naloxégol tablet by oral route
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
inert tablet by oral route
Intervention Type
Drug
Intervention Name(s)
Naloxegol
Intervention Description
one naloxegol 12.5 mg tablet will be administrated 2 hours before surgery. One 25 mg naloxegol tablet per day will be administrated from 24h post-surgery until bowel movement; for maximum 5 days.
Intervention Type
Drug
Intervention Name(s)
inert tablet
Intervention Description
one inert tablet will be administrated 2 hours before surgery. One inert tablet per day will be administrated from 24h post-surgery until bowel movement; for maximum 5 days.
Primary Outcome Measure Information:
Title
Evaluate the effect of perioperative naloxegol administration on the duration of postoperative ileus after cardiac surgery
Description
Time (hour) to transit recovery after cardiac surgery
Time Frame
5 days
Secondary Outcome Measure Information:
Title
Incidence of digestive complications
Description
rate of digestive complications
Time Frame
30 days
Title
Evaluate the effect of the administration of Naloxegol on respiratory complications
Description
rate of respiratory complications
Time Frame
30 days
Title
Evaluate the effect of the administration of Naloxegol on infectious complications
Description
rate of infectious complications
Time Frame
30 days
Title
Verify the effectiveness of analgesia
Description
Pain Visual Analogue Scale (VAS) ranging from 0 to 10 (0=no pain, 10=worst possible pain)
Time Frame
day 1, day2, day3
Title
Compare the length of hospital stay
Description
Duration of hospital stay (days)
Time Frame
30 days
Title
Compare the length of ICU stay
Description
Duration of ICU stay (days)
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: > 18 years old, Undergoing cardiac surgery with cardiopulmonary bypass, For women of child bearing potential without contraception, beta-HCG negative result Having signed a written informed consent form, Affiliation to the social security system. Exclusion Criteria: Allergy or known hypersensitivity to Naloxegol or any of the excipients or any other opioid antagonist Pregnant or breastfeeding women Severe hepatic failure, history of cirrhosis Moderate or severe renal failure (GFR<60ml/min) Concomitant treatment with a strong cytochrome P450 3A4 inhibitor History of acute gastro-intestinal obstruction known or suspected History of digestive arteritis Clinically relevant alteration of the blood-brain-barrier Cancer with increased risk of gastro-duodenal perforation Disorder that could alter the integrity of the gastrointestinal lining Regular treatment with laxative drugs Concomitant treatment with methadone Patient unable to take a drug by oral route Patient under protection of the adults (guardianship, curators or safeguard of justice), Patient included or planning to be included in another research protocol relating to medications.
Facility Information:
Facility Name
CMC Ambroise Paré
City
Neuilly-sur-Seine
State/Province
Neuilly Sur Seine
ZIP/Postal Code
92200
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Effect of Naloxegol on Postoperative Ileus in Patients Undergoing Cardiac Surgery

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