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A Study to Compare Two Techniques for Pain Control After Bariatric Surgery

Primary Purpose

Pain, Postoperative, Bariatric Surgery Candidate

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Transversus Abdominis Plane (TAP) block
Port-Site Infiltration (PSI)
Sponsored by
Fabio Garofalo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pain, Postoperative focused on measuring Transversus Abdominis Plane (TAP) Block, Local Anesthetic Infiltrations

Eligibility Criteria

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

Inclusion Criteria:

  • patients undergoing elective bariatric surgery
  • age ≥ 18 years
  • signed informed consent

Exclusion Criteria:

  • Pregnant or lactating women,
  • known allergy to local anesthetics
  • Chronic pain syndrome.

Sites / Locations

  • Ospedale Regionale di Lugano, Civico e Italiano

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Arm A - laparoscopic assisted TAP block

Arm B - PSI

Arm Description

Patients will undergo the planned bariatric intervention according to the standard of treatment. A solution of 20 ml of the local anesthetic Ropivacaine (0.25%) is then injected for postoperative pain control according to the allocated procedure (TPA).

Patients will undergo the planned bariatric intervention according to the standard of treatment. A solution of 20 ml of the local anesthetic Ropivacaine (0.25%) is then injected for postoperative pain control according to the allocated procedure (PSI).

Outcomes

Primary Outcome Measures

Postoperative Pain
Postoperative pain on the visual analogue scale (VAS) This visual analogue scale measures the subjective pain: patients indicate a position along a continuous line between two end-points to specify their level of pain. Absence of pain is represented by 0 while 10 corresponds to the maximum of pain.

Secondary Outcome Measures

postoperative pain
Postoperative pain on the visual analogue scale (VAS) at 3, 6, 12, 18 hours. This visual analogue scale measures the subjective pain: patients indicate a position along a continuous line between two end-points to specify their level of pain. Absence of pain is represented by 0 while 10 corresponds to the maximum of pain.
Number of Participants With Ropivacaine-Related Adverse Events
Number of participants with complications
Number of participants with complications, defined as any alteration from the normal or uneventful postoperative course,
lenght of hospital stay
number of days the participant is being hospitalized
in hospital satisfaction
In hospital satisfaction (measured on the validated Leiden Perioperative Patient Satisfaction -LPPS - questionnaire for the perioperative patients' satisfaction. This questionnaire assess patient satisfaction with perioperative care. Patients are asked to score each question on a fivepoint scale (from 1 - corresponding to the worse outcome to 5 - the best outcome)

Full Information

First Posted
June 1, 2020
Last Updated
October 5, 2021
Sponsor
Fabio Garofalo
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1. Study Identification

Unique Protocol Identification Number
NCT04427059
Brief Title
A Study to Compare Two Techniques for Pain Control After Bariatric Surgery
Official Title
Laparoscopic Assisted Transversus Abdominis Plane (TAP) Block Vs Local Anesthetic Infiltrations in Bariatric Surgery: a Prospective Randomized Double-Blind Controlled Trial (TAP BLOCK BARIATRIC TRIAL)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
June 15, 2020 (Actual)
Primary Completion Date
July 7, 2021 (Actual)
Study Completion Date
July 7, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Fabio Garofalo

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
The purpose of this study is to compare the postoperative pain and other clinical outcomes in patients who, during bariatric surgery, will be injected with a local anesthetic (Ropivacaine) through two different techniques.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Postoperative, Bariatric Surgery Candidate
Keywords
Transversus Abdominis Plane (TAP) Block, Local Anesthetic Infiltrations

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
115 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm A - laparoscopic assisted TAP block
Arm Type
Experimental
Arm Description
Patients will undergo the planned bariatric intervention according to the standard of treatment. A solution of 20 ml of the local anesthetic Ropivacaine (0.25%) is then injected for postoperative pain control according to the allocated procedure (TPA).
Arm Title
Arm B - PSI
Arm Type
Active Comparator
Arm Description
Patients will undergo the planned bariatric intervention according to the standard of treatment. A solution of 20 ml of the local anesthetic Ropivacaine (0.25%) is then injected for postoperative pain control according to the allocated procedure (PSI).
Intervention Type
Procedure
Intervention Name(s)
Transversus Abdominis Plane (TAP) block
Intervention Description
The laparoscopic-assisted Transversus Abdominis Plane (TAP) block will be done just after the optic trocar placement as follow: as landmarks we use the anterior axillary line, in the middle between the iliac crest and the costal margin. After insertion of the optic trocar the peritoneum is visualized. A 14 Gauge needle is inserted 2 cm cranially respect the taken landmark through the skin until the penetration of the internal and external oblique fascias, identified as sudden lowering of resistance. Laparoscopy allows to confirm that the needle did not pass the peritoneum. A solution of 20 ml of Ropivacaine (0.25%) is then injected, observing the formation of a bulge posterior to the transversus abdominis muscle. The procedure is then repeated identically on the contralateral side.
Intervention Type
Procedure
Intervention Name(s)
Port-Site Infiltration (PSI)
Intervention Description
The Port-Site Infiltration (PSI) will be performed by infiltrating the subcutis and the skin at the trocar site before the trocar placements with a solution of local anesthetic (Ropivacaine 0.25%), a total of 40 ml will be administered.
Primary Outcome Measure Information:
Title
Postoperative Pain
Description
Postoperative pain on the visual analogue scale (VAS) This visual analogue scale measures the subjective pain: patients indicate a position along a continuous line between two end-points to specify their level of pain. Absence of pain is represented by 0 while 10 corresponds to the maximum of pain.
Time Frame
at 24 hours post surgery
Secondary Outcome Measure Information:
Title
postoperative pain
Description
Postoperative pain on the visual analogue scale (VAS) at 3, 6, 12, 18 hours. This visual analogue scale measures the subjective pain: patients indicate a position along a continuous line between two end-points to specify their level of pain. Absence of pain is represented by 0 while 10 corresponds to the maximum of pain.
Time Frame
at 3, 6, 12, 18 hours from surgery
Title
Number of Participants With Ropivacaine-Related Adverse Events
Time Frame
from surgery up to six weeks after surgery
Title
Number of participants with complications
Description
Number of participants with complications, defined as any alteration from the normal or uneventful postoperative course,
Time Frame
from surgery up to six weeks after surgery
Title
lenght of hospital stay
Description
number of days the participant is being hospitalized
Time Frame
during hospitalization,approximately 4 days
Title
in hospital satisfaction
Description
In hospital satisfaction (measured on the validated Leiden Perioperative Patient Satisfaction -LPPS - questionnaire for the perioperative patients' satisfaction. This questionnaire assess patient satisfaction with perioperative care. Patients are asked to score each question on a fivepoint scale (from 1 - corresponding to the worse outcome to 5 - the best outcome)
Time Frame
during hospitalization,approximately 4 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients undergoing elective bariatric surgery age ≥ 18 years signed informed consent Exclusion Criteria: Pregnant or lactating women, known allergy to local anesthetics Chronic pain syndrome.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fabio Garofalo, MD
Organizational Affiliation
EOC Surgeery Department
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ospedale Regionale di Lugano, Civico e Italiano
City
Lugano
ZIP/Postal Code
6900
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No

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A Study to Compare Two Techniques for Pain Control After Bariatric Surgery

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