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Botulinum Toxin Pyloroplasty to Reduce Postoperative Nausea and Vomiting After Sleeve Gastrectomy

Primary Purpose

Bariatric Surgery, Postoperative Nausea and Vomiting

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Botulinum toxin pyloroplasty
Normal saline pyloric injection
Sponsored by
Albany Medical College
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bariatric Surgery

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • Patients undergoing elective sleeve gastrectomy

Exclusion criteria:

  • Prior gastric surgery resulting in altered anatomy
  • Documented history of postoperative nausea or vomiting
  • Allergy to any of the medications used in the study
  • Any use of Botulinum toxin products within six months prior to study enrollment, or plans to use Botulinum toxin products during study enrollment

Sites / Locations

  • Albany Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Botulinum toxin pyloroplasty

Normal saline pyloric injection

Arm Description

Intraoperative laparoscopic intramuscular injection of 100units (10cc) of Botulinum toxin into the pylorus

Intraoperative laparoscopic intramuscular injection of 10cc normal saline into the pylorus

Outcomes

Primary Outcome Measures

Use of rescue antiemetics
We will sum the number of "as needed" doses of intravenous antiemetics required by patients in both the treatment arm and the control arm of the study

Secondary Outcome Measures

Patient satisfaction survey
Likert scales describing overall satisfaction with postoperative course
Subjective experience of nausea
Likert score rating subjective experience of nausea
Number of episodes of vomiting
Number of episodes of emesis
30 day readmission rate
30 day readmission rate
Hospital length of stay
Hospital length of stay

Full Information

First Posted
October 1, 2018
Last Updated
April 7, 2023
Sponsor
Albany Medical College
Collaborators
Allergan
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1. Study Identification

Unique Protocol Identification Number
NCT03701919
Brief Title
Botulinum Toxin Pyloroplasty to Reduce Postoperative Nausea and Vomiting After Sleeve Gastrectomy
Official Title
Botulinum Toxin Pyloroplasty to Reduce Postoperative Nausea and Vomiting After Sleeve Gastrectomy
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
January 7, 2019 (Actual)
Primary Completion Date
November 11, 2022 (Actual)
Study Completion Date
November 11, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Albany Medical College
Collaborators
Allergan

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.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A common problem following sleeve gastrectomy surgery is called postoperative nausea and vomiting (PONV). This problem is uncomfortable for patients, and can also lead to other complications, including pneumonia. It is unclear what exactly causes this problem, but it may be partly caused by slow emptying of the stomach. The current treatments for PONV include medications, but these may only treat the symptoms. Botulinum toxin (BTX, brand name Botox®), produced naturally by the bacterium Clostridium botulinum and adapted for medical use, is an neurotransmitter inhibitor of the neuromuscular junction, and produces temporary muscular paralysis. BTX is widely used in cosmetic and other medical applications. Injecting BTX into the pylorus, which is the circular sphincter muscle at the end of the stomach, temporarily paralyzes the muscle, leaving it wide open, and allowing stomach contents to flow through. This effect lasts for several weeks, and then goes away. This may help prevent PONV.
Detailed Description
Postoperative nausea and vomiting (PONV) remains a common complaint after bariatric surgery such as the sleeve gastrectomy, where the prevalence is estimated to be as high as 60-80%. PONV is frequently of greater concern to patients than postoperative pain, decreasing patient satisfaction and the perioperative experience. In addition, PONV increases the risk for aspiration, dehydration, electrolyte abnormalities, incisional dehiscence, esophageal injury, and other adverse events. Finally, PONV delays postoperative diet resumption and increases hospital length of stay. Numerous medication regimens have been tried to reduce PONV after sleeve gastrectomy, with varying success. A procedure called Botulinum toxin pyloroplasty (BP), which involves injection of botulinum toxin into the muscular sphincter at the end of the stomach, called the pylorus, has been demonstrated to improve gastric emptying. The investigators hypothesize that intraoperative BP during sleeve gastrectomy will decrease rates of PONV. Botulinum toxin type A (Botox®), produced naturally by the bacterium Clostridium botulinum and adapted for medical use, is an inhibitor of the neurotransmitter acetylcholine at the neuromuscular junction, producing flaccid muscular paralysis. The effects of Botox® injection are temporary and reversible, and its duration of action ranges from weeks to months. Botox® injection has been widely used in many contexts, most familiarly during office-based cosmetic procedures and also in disorders such as torticollis, spasticity, hyperhidrosis, bladder overreactivity, and dystonias. It has been used endoscopically to relieve achalasia and dysphagia by injection into the lower esophageal sphincter. Gastroenterologists have reported successful treatment of gastroparesis using BP, by relieving the tonic contraction of the pylorus and increasing gastric transit time. Postoperative endoscopic BP has been utilized to improve gastroparesis following gastrectomy. The use of BP during bariatric surgery has not been reported. This proposal represents the first study to evaluate the use of intraoperative BP to decrease PONV after sleeve gastrectomy. This technique involves pyloroplasty following completion of the robot-assisted laparoscopic sleeve gastrectomy. The investigators mix 100 units of Botox® powder in 10ml of saline. Using the robot, the investigators inject the pylorus laparoscopically using an 18-gauge, 0.5-inch laparoscopic needle. Meanwhile, an assistant surgeon intubates the stomach with an endoscope, which the investigators use to assess the gastric staple line and perform a leak test. Prior to injection of Botox® into the pylorus, the investigators confirm endoscopically that the tip of the needle is not intraluminal. After first aspirating to ensure the needle is intramuscular and free from any vascular structures, the investigators then inject the pylorus with approximately 5ml of Botox®. Proper placement of the injection is confirmed by visualizing a rising weal. The anterior, superior, and inferior aspects of the pylorus are injected with approximately 5-6 injections of 1ml each. The posterior aspect of the pylorus is not injected, since this is not readily accessible from a laparoscopic approach, and also contains the major vascular structure of the pylorus, the gastroduodenal artery. This technique has been performed at Albany Medical Center institution more than 200 times over the past four years. The Albany Medical Center Bariatric Center as participated in the Metabolic and Bariatric Surgery Accreditation for 10 years, and so has collected comprehensive and granular data on complication rates and surgical outcomes. Analysis of this data demonstrates that enteric use of Botox® is safe.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bariatric Surgery, Postoperative Nausea and Vomiting

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
84 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Botulinum toxin pyloroplasty
Arm Type
Experimental
Arm Description
Intraoperative laparoscopic intramuscular injection of 100units (10cc) of Botulinum toxin into the pylorus
Arm Title
Normal saline pyloric injection
Arm Type
Placebo Comparator
Arm Description
Intraoperative laparoscopic intramuscular injection of 10cc normal saline into the pylorus
Intervention Type
Drug
Intervention Name(s)
Botulinum toxin pyloroplasty
Other Intervention Name(s)
Botox pyloropasty, Botulinum toxin A pyloroplasty
Intervention Description
Intraoperative laparoscopic injection of Botulinum toxin into the pylorus immediately following sleeve gastrectomy
Intervention Type
Drug
Intervention Name(s)
Normal saline pyloric injection
Intervention Description
Intraoperative laparoscopic injection of normal saline into the pylorus immediately following sleeve gastrectomy
Primary Outcome Measure Information:
Title
Use of rescue antiemetics
Description
We will sum the number of "as needed" doses of intravenous antiemetics required by patients in both the treatment arm and the control arm of the study
Time Frame
During inpatient hospitalization only, an average of 2-3 days
Secondary Outcome Measure Information:
Title
Patient satisfaction survey
Description
Likert scales describing overall satisfaction with postoperative course
Time Frame
2 weeks postoperative
Title
Subjective experience of nausea
Description
Likert score rating subjective experience of nausea
Time Frame
2 weeks postoperative
Title
Number of episodes of vomiting
Description
Number of episodes of emesis
Time Frame
2 weeks postoperative
Title
30 day readmission rate
Description
30 day readmission rate
Time Frame
30 days postoperative
Title
Hospital length of stay
Description
Hospital length of stay
Time Frame
During inpatient hospitalization only, an average of 2-3 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Patients undergoing elective sleeve gastrectomy Exclusion criteria: Prior gastric surgery resulting in altered anatomy Documented history of postoperative nausea or vomiting Allergy to any of the medications used in the study Any use of Botulinum toxin products within six months prior to study enrollment, or plans to use Botulinum toxin products during study enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jessica Zaman, MD
Organizational Affiliation
Albany Medical College
Official's Role
Principal Investigator
Facility Information:
Facility Name
Albany Medical Center
City
Albany
State/Province
New York
ZIP/Postal Code
12208
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Botulinum Toxin Pyloroplasty to Reduce Postoperative Nausea and Vomiting After Sleeve Gastrectomy

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