Sugammadex To IMprove Bowel Function (STIM_Bowel)
Primary Purpose
Bowel Dysfunction, Postoperative Complications, Neuromuscular Blockade
Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Sugammadex
Neostigmine
Sponsored by
About this trial
This is an interventional prevention trial for Bowel Dysfunction focused on measuring sugammadex, neostigmine, Gastric emptying, neuromuscular blockade
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years
- Having surgery in the South Operating Rooms at Oregon Health & Science University
- Surgery scheduled Monday through Friday
- Having colorectal surgery
- Planned general endotracheal anesthesia
Exclusion Criteria:
- Prisoners
- Pregnant women
- An inability to consent for surgery or anesthesia
- Allergy to a study drug
- Medical contraindication to neuromuscular blockade
- Stage 4 kidney disease or worse (glomerular filtration rate < 30 ml/min)
- Significant liver dysfunction (Aspartate transaminase or Alanine transaminase > twice the OHSU normal)
- Taking Toremifene
Sites / Locations
- Oregon Health & Science UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Sugammadex
Neostigmine
Arm Description
Sugammadex 2 mg/kg IV once at the end of surgery
Neostigmine 0.07 mg/kg to a maximum of 5 mg (+Glycopyrrolate 0.2 mg per 1 mg of neostigmine administered) IV once at the end of surgery
Outcomes
Primary Outcome Measures
Gastric emptying
Gastric emptying as assessed by the area under the paracetamol concentration-time curve by trapezoidal approximation (AUC)
Secondary Outcome Measures
Time in minutes to reach train of four (TOF) ratio ≥ 0.9 after the administration of reversal drug.
The TOF ratio will be measured in continuous manner every 15 seconds after the administration of reversal drug. The TOF ratio will be measured by the TwitchView electromyograph.
Full Information
NCT ID
NCT04546672
First Posted
September 5, 2020
Last Updated
September 22, 2022
Sponsor
Oregon Health and Science University
Collaborators
Merck Sharp & Dohme LLC
1. Study Identification
Unique Protocol Identification Number
NCT04546672
Brief Title
Sugammadex To IMprove Bowel Function
Acronym
STIM_Bowel
Official Title
An Assessor-blinded, Randomized, Controlled, Single Center, Parallel Design Trial With Patient Masking to Compare Early Postoperative Gastric Emptying Associated With Rocuronium Neuromuscular Reversal With Sugammadex Versus Neostigmine in Adults Undergoing Colon and Rectal Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 16, 2021 (Actual)
Primary Completion Date
July 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oregon Health and Science University
Collaborators
Merck Sharp & Dohme LLC
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
Colon and rectal surgery is associated with high cost, long length of stay, high postoperative surgical site infection rate, high incidence of postoperative nausea and vomiting, and a high rate of hospital readmission. Return of bowel function is of utmost importance in avoiding patient discomfort, morbidity, and mortality after colorectal surgery. All patient having colorectal surgery receive neuromuscular paralysis, which is reversed at the end of surgery with either glycopyrrolate and neostigmine, or sugammadex. Glycopyrrolate and neostigmine both affect bowel function. Sugammadex has no effect on bowel function. The purpose of this study is to determine if a strategy of neuromuscular reversal with sugammadex, instead of glycopyrrolate and neostigmine, may increase gastric emptying after surgery and lead to less postoperative complications.
Detailed Description
Colon and rectal surgery is associated with high cost, long length of stay, high postoperative surgical site infection rate, high incidence of postoperative nausea and vomiting, and a high rate of hospital readmission. The 30-day mortality rate after open or laparoscopic surgery for colorectal cancer is high-between 3 and 8%. Return of bowel function is of utmost importance in avoiding patient discomfort, morbidity, and mortality after colorectal surgery. The incidence of postoperative ileus after colorectal surgery has been reported to be 10-25%. Postoperative ileus is defined as intolerance of oral intake due to a lack of coordinated bowel motility. Significant attention has been paid to the development of guidelines and programs to reduce the incidence of postoperative ileus and accelerate return of bowel function after colorectal surgery.
The American Society of Colon and Rectal Surgeons (ASCRS) and the Society of American Gastrointestinal and Endoscopic Surgeons (SAGES) created an enhanced recovery after surgery (ERAS) protocol to promote the following outcomes in patients undergoing colorectal surgery: "freedom from nausea, freedom from pain at rest, early return of bowel function, improved wound healing, and early hospital discharge". An intervention that facilitates faster postoperative gastric emptying may impact many of these outcomes; in particular, nausea may be reduced, constipation-associated pain at rest may decline, return of bowel function would be accelerated, and time to hospital discharge may be shortened. While administration of medications such as Alvimopan and adjustments in anesthetic technique (providing epidural analgesia, minimizing crystalloid administration, using multimodal analgesia) are recommended, sugammadex is not currently considered in the ERAS protocol.
Neuromuscular paralysis is required for the duration of open and laparoscopic colorectal surgery to decrease patient movement, improve operating conditions, and at times facilitate ventilation. Neostigmine and glycopyrrolate are commonly used to reverse rocuronium neuromuscular blockade at the end of surgery. Both neostigmine and glycopyrrolate impact bowel function. Neostigmine promotes and glycopyrrolate slows gastrointestinal motility. Co-administration of neostigmine and glycopyrrolate can have variable effects on return of bowel function after surgery. In general, administering a higher proportion of neostigmine than glycopyrrolate is associated with faster return of bowel function. Unopposed cholinergic activity from neostigmine administration can cause morbidity including bradycardia, bronchoconstriction, hypotension, urinary incontinence, and increased salivary secretions. Thus, the ratio of neostigmine to glycopyrrolate is relatively fixed and cannot be adjusted to promote desired gastrointestinal outcomes. Sugammadex does not bind to acetylcholine receptors on bowel and is presumed not to affect bowel function.
Some investigations into the contribution of sugammadex versus acetylcholinesterase inhibitors to recovery of bowel function have been completed. In retrospective studies, sugammadex administration has been associated with faster time to first bowel movement and less ileus-related delays in hospital discharge. Conversely, two randomized, controlled clinical trials found no difference in outcomes related to gastrointestinal motility including time to first flatus, time to first bowel movement, and incidence of postoperative ileus. One randomized, controlled trial found a shorter time to first flatus, but no difference in time to first bowel movement. Lastly, one study found a trend towards faster gastric emptying with sugammadex. A limitation of the aforementioned prospective studies is they include patients having surgery on their thyroid gland, gallbladder, and other intraabdominal organs. These surgeries lack bowel handling and anastomosis, which translates to less effect on postoperative bowel function. It is hypothesized that a randomized, controlled trial involving patients having colorectal surgery will find faster gastric emptying, less nausea, and less gastrointestinal complications (including ileus) when sugammadex is administered to reverse rocuronium neuromuscular blockade, compared to neostigmine.
The purpose of this study is to determine if administering sugammadex for reversal of neuromuscular blockade instead of neostigmine and glycopyrrolate, a strategy that avoids cholinergic effects on the bowel, is associated with faster gastric emptying, faster time to achieve a TOFr > 0.9, less post-surgical gastrointestinal complications, shorter time to first bowel movement, shorter PACU phase 1 recovery, and shorter hospital length of stay. If sugammadex is shown to improve the aforementioned outcomes, an argument can be made that sugammadex should be considered for inclusion in the ERAS protocol for Colorectal surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bowel Dysfunction, Postoperative Complications, Neuromuscular Blockade
Keywords
sugammadex, neostigmine, Gastric emptying, neuromuscular blockade
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Assessor-blinded, randomized, controlled, single center, parallel design trial with patient masking
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Sugammadex
Arm Type
Experimental
Arm Description
Sugammadex 2 mg/kg IV once at the end of surgery
Arm Title
Neostigmine
Arm Type
Active Comparator
Arm Description
Neostigmine 0.07 mg/kg to a maximum of 5 mg (+Glycopyrrolate 0.2 mg per 1 mg of neostigmine administered) IV once at the end of surgery
Intervention Type
Drug
Intervention Name(s)
Sugammadex
Other Intervention Name(s)
Org 25969, Bridion
Intervention Description
At the end of the surgical procedure at a depth of neuromuscular blockade after the reappearance of T2 on the train-of-four, Sugammadex will be dosed once at 2 mg/kg actual body weight through an intravenous line with brisk flow
Intervention Type
Drug
Intervention Name(s)
Neostigmine
Other Intervention Name(s)
Prostigmin, Vagostigmin
Intervention Description
At the end of surgical procedure at a depth of neuromuscular blockade after the reappearance of T2 on the train-of-four, Neostigmine will be dosed once at 0.07 mg/kg actual body weight to a maximum of 5 mg through an intravenous line with brisk flow. Glycopyrrolate will be coadministered with Neostigmine at a dose of 0.2 mg of Glycopyrrolate per 1.0 mg of Neostigmine administered
Primary Outcome Measure Information:
Title
Gastric emptying
Description
Gastric emptying as assessed by the area under the paracetamol concentration-time curve by trapezoidal approximation (AUC)
Time Frame
0, 15, 30, 45, 60, 90, 120, and 150 minutes after neuromuscular reversal
Secondary Outcome Measure Information:
Title
Time in minutes to reach train of four (TOF) ratio ≥ 0.9 after the administration of reversal drug.
Description
The TOF ratio will be measured in continuous manner every 15 seconds after the administration of reversal drug. The TOF ratio will be measured by the TwitchView electromyograph.
Time Frame
30 minutes after the administration of reversal drug.
Other Pre-specified Outcome Measures:
Title
Gastrointestinal complications
Description
Gastrointestinal complications will include all of the following: anastomotic leak, postoperative ileus, reoperation, and organ space infection. National Surgical Quality Improvement Project definitions will be used. Active monitoring for these outcomes will occur on an ongoing daily basis until hospital discharge. In addition, chart review and patient phone call will occur 30-60 days after discharge to assess for complications after discharge.
Time Frame
60 days after surgery
Title
Bowel movement
Description
The time to first bowel movement after surgery
Time Frame
length hospitalization, an average of 1 week
Title
PACU phase 1 recovery time
Description
The time to attain pain control and stable respiratory, hemodynamic, and neurologic status after surgery.
Time Frame
1 day
Title
Hospital length of stay
Description
The number of days between hospital admission and hospital discharge
Time Frame
length of hospitalization, an average of 1 week
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18 years
Having surgery in the South Operating Rooms at Oregon Health & Science University
Surgery scheduled Monday through Friday
Having colorectal surgery
Planned general endotracheal anesthesia
Exclusion Criteria:
Prisoners
Pregnant women
An inability to consent for surgery or anesthesia
Allergy to a study drug
Medical contraindication to neuromuscular blockade
Stage 4 kidney disease or worse (glomerular filtration rate < 30 ml/min)
Significant liver dysfunction (Aspartate transaminase or Alanine transaminase > twice the OHSU normal)
Taking Toremifene
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sarah Feller
Phone
503-494-6233
Email
fellersa@ohsu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Hillary Regan
Phone
503-494-7229
Email
reganh@ohsu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brandon M Togioka, MD
Organizational Affiliation
Oregon Health and Science University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oregon Health & Science University
City
Portland
State/Province
Oregon
ZIP/Postal Code
97239
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sarah Feller
Phone
503-494-6233
Email
fellersa@ohsu.edu
First Name & Middle Initial & Last Name & Degree
Hillary Regan
Phone
503-494-7229
Email
reganh@ohsu.edu
First Name & Middle Initial & Last Name & Degree
Brandon M Togioka, MD
12. IPD Sharing Statement
Plan to Share IPD
No
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Sugammadex To IMprove Bowel Function
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