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Ropivacaine For Post-POEM Pain Control

Primary Purpose

Achalasia, Esophageal Achalasia

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Ropivacaine
Normal saline
Sponsored by
Lawrence Charles Hookey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Achalasia focused on measuring Peroral Endoscopic Myotomy, Ropivacaine, Post-procedure pain control

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years of age and older undergoing POEM procedure
  • Able to provide written informed consent
  • Fluent and literate in English

Exclusion Criteria:

  • Patients with known adverse reactions to local anesthetics and NSAIDs (GFR<50)
  • Patients with chronic pain taking regular analgesics or narcotics (requiring daily opioid therapy > 30 mg morphine or equivalents)
  • Patients unable to give informed consent

Sites / Locations

  • Kingston Health Sciences Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Ropivacaine

Normal Saline

Arm Description

30mL of 0.2% Ropivacaine placed in the POEM tunnel

30mL of normal saline placed in the POEM tunnel

Outcomes

Primary Outcome Measures

Post-POEM pain level
To assess the effect of the intervention/placebo on pain 6-hours post-POEM as assessed via the Numeric Rating Scale (NRS): The patient will be asked to rate their pain on a scale of 0-10, 0 representing no pain, and 10 representing the worst pain they have ever felt in their life.

Secondary Outcome Measures

Post-POEM pain level
Assessing pain scores at 0, 0.5, 1, 2, 4 hours post-POEM and on discharge
Quality of Recovery (QoR-15) score on the day of discharge
Quality of Recovery-15 score: This survey captures patient's initial post-operative health condition and their overall patient experience. The patient will be asked to rate various emotional and physical aspects of their post-operative condition on a scale of 0-10. 0 will represent an emotion or activity experienced or accomplished none of the time, and 10 will represent an emotion or activity accomplished all of the time. Scores are summed; higher scores indicate a more optimal post-operative condition.
Post-POEM analgesic
The requirement of post-POEM analgesic
Adverse Events
Adverse events in hospital
Fentanyl consumption
Intraprocedural fentanyl consumption
Repeatability of procedure
Patient's willingness to have the procedure done on an outpatient basis: Patients will be asked if they are "willing" or "not willing" to have the procedure done on an outpatient basis.

Full Information

First Posted
October 4, 2018
Last Updated
January 25, 2021
Sponsor
Lawrence Charles Hookey
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1. Study Identification

Unique Protocol Identification Number
NCT03702647
Brief Title
Ropivacaine For Post-POEM Pain Control
Official Title
Ropivacaine For Post-POEM Pain Control
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
June 1, 2019 (Actual)
Primary Completion Date
December 1, 2020 (Actual)
Study Completion Date
January 18, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Lawrence Charles Hookey

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
POEM (Peroral Endoscopic Myotomy) is an endoscopic procedure most commonly used to treat achalasia. Achalasia is a disorder resulting from the inability of esophageal muscles to relax.The POEM procedure, performed under general anesthesia, involves inserting an endoscope into the esophagus where a specialized knife is able to cut a new pathway through the esophageal tissue. The knife is then used to incise, and therefore loosen, tight muscles within the esophagus, lower esophageal sphincter, and the upper region of the stomach that are responsible for the symptoms.This study seeks to improve patient's post-operative pain levels by placing ropivacaine (a local anesthetic) into the newly cut pathway that is created in the POEM procedure. It is hypothesized that the topical irrigation of the POEM tunnel with ropivacaine will result in decreased pain scores and a decreased need for additional pain medications.
Detailed Description
POEM (Peroral Endoscopic Myotomy) is an endoscopic procedure most commonly used to treat achalasia. Achalasia is a disorder resulting from the inability of esophageal muscles to relax. Consequently, patients experience difficulty swallowing, reflux, and weight loss. Treatment options for achalasia are generally divided into 2 categories: A) treatment with medication, or B) treatment via a procedure. Medical treatment is generally reserved for patients to unwell to undergo procedures as the efficacy is low. Additionally, patients tend to experience many side-effects. There are also procedural options used to treat achalasia which include surgical myotomy and POEM. The POEM procedure is advantageous because it is less invasive, but is at least as equally effective for symptomatic relief when compared to the surgical myotomy. The POEM procedure, performed under general anesthesia, involves inserting an endoscope into the esophagus where a specialized knife is able to cut a new pathway through the esophageal tissue. The knife is then used to incise, and therefore loosen, tight muscles within the esophagus, lower esophageal sphincter, and the upper region of the stomach that are responsible for the symptoms. At the conclusion of the procedure, clips are placed in the esophagus to close the incision. Currently, patients are given intravenous ketorolac, oral viscous lidocaine and narcotic analgesics as needed to manage post-operative pain. This study, however, seeks to improve patient's post-operative pain levels by placing ropivacaine (a local anesthetic) into the newly cut pathway that is created in the POEM procedure. It is hypothesized that the topical irrigation of the POEM tunnel with ropivacaine will result in decreased pain scores and a decreased need for additional pain medications. Patients consented to participate in the study will be randomized to receive either ropivacaine (intervention group) or saline (control group). Pain will be assessed at 0.5, 1, 2, 4, and 6 hours post-admission to the recovery unit using validated pain scales. Additionally, the Quality of Recovery (QoR-15) patient survey, will be completed prior to discharge. This measure will capture the patient's initial post-operative health condition and help capture the overall patient experience.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Achalasia, Esophageal Achalasia
Keywords
Peroral Endoscopic Myotomy, Ropivacaine, Post-procedure pain control

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients enrolled in the study will be randomized to receive either 30mL of normal saline (placebo), or 30mL of 0.2% ropivacaine in the POEM tunnel.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Patients will be randomized by an independent research pharmacist to receive either 30mL 0.2% ropivacaine or 30mL of placebo (saline), both being clear, colorless solutions. These samples will be prepared by the research pharmacist 2-3 weeks prior to the procedure and stored until the procedure date as per pharmacy standards. On the morning of the procedure, the study solution will be taken to the operating room with the patient. During the POEM procedure, prior to closure of the mucosotomy, the study solution is instilled into the tunnel. The investigator, patient, care provider, and research coordinator will be blinded to the group assignment.
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ropivacaine
Arm Type
Experimental
Arm Description
30mL of 0.2% Ropivacaine placed in the POEM tunnel
Arm Title
Normal Saline
Arm Type
Placebo Comparator
Arm Description
30mL of normal saline placed in the POEM tunnel
Intervention Type
Drug
Intervention Name(s)
Ropivacaine
Intervention Description
30mL of 0.2% Ropivacaine placed in the POEM tunnel
Intervention Type
Drug
Intervention Name(s)
Normal saline
Intervention Description
30mL of normal saline placed in the POEM tunnel
Primary Outcome Measure Information:
Title
Post-POEM pain level
Description
To assess the effect of the intervention/placebo on pain 6-hours post-POEM as assessed via the Numeric Rating Scale (NRS): The patient will be asked to rate their pain on a scale of 0-10, 0 representing no pain, and 10 representing the worst pain they have ever felt in their life.
Time Frame
6 hours post-POEM procedure
Secondary Outcome Measure Information:
Title
Post-POEM pain level
Description
Assessing pain scores at 0, 0.5, 1, 2, 4 hours post-POEM and on discharge
Time Frame
0, 0.5, 1, 2, 4 hours post-POEM procedure
Title
Quality of Recovery (QoR-15) score on the day of discharge
Description
Quality of Recovery-15 score: This survey captures patient's initial post-operative health condition and their overall patient experience. The patient will be asked to rate various emotional and physical aspects of their post-operative condition on a scale of 0-10. 0 will represent an emotion or activity experienced or accomplished none of the time, and 10 will represent an emotion or activity accomplished all of the time. Scores are summed; higher scores indicate a more optimal post-operative condition.
Time Frame
Assessed up to 24 hours post-POEM procedure
Title
Post-POEM analgesic
Description
The requirement of post-POEM analgesic
Time Frame
0 -6 hours post-procedure
Title
Adverse Events
Description
Adverse events in hospital
Time Frame
Assessed up to 24 hours post-POEM procedure
Title
Fentanyl consumption
Description
Intraprocedural fentanyl consumption
Time Frame
Intra-procedure
Title
Repeatability of procedure
Description
Patient's willingness to have the procedure done on an outpatient basis: Patients will be asked if they are "willing" or "not willing" to have the procedure done on an outpatient basis.
Time Frame
Assessed 24 hours post-POEM procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years of age and older undergoing POEM procedure Able to provide written informed consent Fluent and literate in English Exclusion Criteria: Patients with known adverse reactions to local anesthetics and NSAIDs (GFR<50) Patients with chronic pain taking regular analgesics or narcotics (requiring daily opioid therapy > 30 mg morphine or equivalents) Patients unable to give informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Bechara, M.D.
Organizational Affiliation
Queens University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kingston Health Sciences Centre
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 5G2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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Ropivacaine For Post-POEM Pain Control

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