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The Effect of Low Pressure Pneumoperitoneum During Laparoscopic Colorectal Surgery on Early Quality of Recovery (RECOVER)

Primary Purpose

Pneumoperitoneum, Neuromuscular Blockade, Surgery

Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Low pressure pneumoperitoneum
Rocuronium Bromide
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pneumoperitoneum focused on measuring Quality of recovery, Laparoscopic surgery, Deep neuromuscular block, Low pressure pneumoperitoneum

Eligibility Criteria

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

Inclusion Criteria:

  • Scheduled for laparoscopic colorectal surgery with a primary anastomosis
  • Obtained informed consent
  • Age over 18 years

Exclusion Criteria:

  • Insufficient control of the Dutch language to read the patient information and to fill out the questionnaires
  • Primary colostomy
  • Neo-adjuvant chemotherapy
  • Chronic use of analgesics or psychotropic drugs
  • Use of NSAIDs shorter than 5 days before surgery
  • Known or suspected allergy to rocuronium of sugammadex
  • Neuromuscular disease
  • Indication for rapid sequence induction
  • Severe liver- or renal disease (creatinine clearance <30ml/min)
  • BMI >35 kg/m²
  • Deficiency of vitamin K dependent clotting factors or coagulopathy

Sites / Locations

  • Canisius Wilhelmina Hospital
  • Martini general hospital
  • Maxima Medisch Centrum

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Low pressure PNP, deep NMB

Normal pressure PNP, moderate NMB

Arm Description

Low pressure pneumoperitoneum of 8 mmHg with deep neuromuscular block (post tetanic count of 1-2) reached by titration with continuous infusion of Rocuronium bromide.

Normal pressure pneumoperitoneum of 12 mmHg with moderate neuromuscular block (TOF count of 1-2) reached by titration with bolus or continuous infusion of a low dose of Rocuronium bromide.

Outcomes

Primary Outcome Measures

Total score on the Quality of Recovery-40 questionnaire
The QoR-40 is a validated assessment tool for measuring a patient's self-assessed quality of recovery after surgery. It consists of 40 questions measuring 5 dimensions: patient support, comfort, emotions, physical independence and pain. Each item is rated on a scale of 1 to 5, giving a minimal score of 40 and a maximum score of 200.

Secondary Outcome Measures

Total score on the Quality of Recovery-40 questionnaire
The QoR-40 is a validated assessment tool for measuring a patient's self-assessed quality of recovery after surgery. It consists of 40 questions measuring 5 dimensions: patient support, comfort, emotions, physical independence and pain. Each item is rated on a scale of 1 to 5, giving a minimal score of 40 and a maximum score of 200.
McGill pain Questionnaire
Validated questionnaire for the assessment of quality and intensity of pain
RAND-36 general health questionnaire
Validated patient-reported survey of health
Pain scores
Pain at rest and pain upon movement (NRS 0-10), is pain acceptable yes or no, referred shoulder pain yes or no?
Post-operative nausea and vomiting (PONV)
NRS 0-10
Cumulative use of analgesics and anti-emetics
Total dose of opiates, other analgesics and anti-emetic drugs
Length of hospital stay
Total number of days from admission to discharge after surgery (not including readmission)
Surgical conditions
Rating of the surgical conditions with the Leiden Surgical Rating Scale (L-SRS). The L-SRS is scored by the surgeon and ranges from 1-5 for quality of the surgical field. A score of 5 means optimal conditions: a wide laparoscopic field with no patient movements or muscle contractions, 1 means extremely poor conditions: the surgeon is unable to obtain a visible laparoscopic field because of inadequate muscle relaxation.
Intraoperative complications
Complications during surgery graded according to the Clavien-Dindo classification
Postoperative complications
Postoperative complications
Time to reach discharge criteria
Number of days to reach the following criteria after surgery: adequate pain control with oral medication, passage of flatus or defecation, intake of solid food tolerated, patient is mobilized and independent and patient accepts discharge.

Full Information

First Posted
June 18, 2018
Last Updated
October 27, 2021
Sponsor
Radboud University Medical Center
Collaborators
Merck Sharp & Dohme LLC
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1. Study Identification

Unique Protocol Identification Number
NCT03608436
Brief Title
The Effect of Low Pressure Pneumoperitoneum During Laparoscopic Colorectal Surgery on Early Quality of Recovery
Acronym
RECOVER
Official Title
RECOVER Study: the Effect of Low- Versus Normal Pressure Pneumoperitoneum During Laparoscopic Colorectal Surgery on the Early Quality of Recovery With Perioperative Care According to the Enhanced Recovery Principles
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
October 24, 2018 (Actual)
Primary Completion Date
March 3, 2021 (Actual)
Study Completion Date
June 3, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
Collaborators
Merck Sharp & Dohme LLC

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
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
Randomised controlled trial comparing the effect of low pressure pneumoperitoneum with deep neuromuscular block versus normal pressure pneumoperitoneum with moderate neuromuscular block during laparoscopic colorectal surgery on early quality of recovery.
Detailed Description
Rationale: the laparoscopic approach reduced trauma as compared to open surgery, however, the pressure used to create a PNP with sufficient surgical workspace still leads to significant tissue injury. Prior studies show that the use of low-pressure pneumoperitoneum (PNP) during laparoscopic surgery reduced postoperative pain scores, cumulative opioid consumption and improved bowel function recovery. Deep neuromuscular blockade (NMB) as compared to moderate NMB decreases the amount of intra-abdominal pressure required to achieve similar surgical conditions and enables the use of low-pressure PNP without compromising the quality of the surgical field and patient safety. Therefore, the use of deep NMB with low-pressure PNP could be a significant addition to the conventional Enhanced Recovery After Surgery (ERAS) protocols. Objective: to establish the relationship between the use of low pressure pneumoperitoneum with deep neuromuscular blockade and the early quality of recovery after laparoscopic colorectal surgery. Study design: a multi-center, blinded, randomized controlled clinical trial. Study population: adult individuals scheduled for laparoscopic colorectal surgery with a primary colonic anastomosis. Intervention: participants will be randomly assigned in a 1:1 fashion to either the experimental group (group A): low pressure PNP (8 mmHg) with deep NMB (PTC 1-2) or the control group (group B): normal pressure PNP (12 mmHg) with moderate NMB (TOF count 1-2). Primary endpoint: Quality of recovery score (QoR-40) 24 hours after surgery. Secondary endpoints: QoR-40 score (day 3 and 7 after surgery), McGill pain- and RAND-36 score (1 day before and 3 months after surgery), pain scores, PONV, analgesia use, length of hospital stay, postoperative complications, surgical conditions and time to reach discharge criteria.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pneumoperitoneum, Neuromuscular Blockade, Surgery
Keywords
Quality of recovery, Laparoscopic surgery, Deep neuromuscular block, Low pressure pneumoperitoneum

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Low pressure PNP, deep NMB
Arm Type
Experimental
Arm Description
Low pressure pneumoperitoneum of 8 mmHg with deep neuromuscular block (post tetanic count of 1-2) reached by titration with continuous infusion of Rocuronium bromide.
Arm Title
Normal pressure PNP, moderate NMB
Arm Type
Active Comparator
Arm Description
Normal pressure pneumoperitoneum of 12 mmHg with moderate neuromuscular block (TOF count of 1-2) reached by titration with bolus or continuous infusion of a low dose of Rocuronium bromide.
Intervention Type
Procedure
Intervention Name(s)
Low pressure pneumoperitoneum
Other Intervention Name(s)
Low intra-abdominal pressure
Intervention Description
Lowering intra-abdominal pressure during laparoscopic surgery
Intervention Type
Drug
Intervention Name(s)
Rocuronium Bromide
Other Intervention Name(s)
Deep muscle relaxation
Intervention Description
Deep (PTC 1-2) versus moderate (Tof count 1-2) neuromuscular block
Primary Outcome Measure Information:
Title
Total score on the Quality of Recovery-40 questionnaire
Description
The QoR-40 is a validated assessment tool for measuring a patient's self-assessed quality of recovery after surgery. It consists of 40 questions measuring 5 dimensions: patient support, comfort, emotions, physical independence and pain. Each item is rated on a scale of 1 to 5, giving a minimal score of 40 and a maximum score of 200.
Time Frame
24 hours after surgery
Secondary Outcome Measure Information:
Title
Total score on the Quality of Recovery-40 questionnaire
Description
The QoR-40 is a validated assessment tool for measuring a patient's self-assessed quality of recovery after surgery. It consists of 40 questions measuring 5 dimensions: patient support, comfort, emotions, physical independence and pain. Each item is rated on a scale of 1 to 5, giving a minimal score of 40 and a maximum score of 200.
Time Frame
Day 3 and day 7 after surgery
Title
McGill pain Questionnaire
Description
Validated questionnaire for the assessment of quality and intensity of pain
Time Frame
Upon admission and 3 months after surgery
Title
RAND-36 general health questionnaire
Description
Validated patient-reported survey of health
Time Frame
Upon admission and 3 months after surgery
Title
Pain scores
Description
Pain at rest and pain upon movement (NRS 0-10), is pain acceptable yes or no, referred shoulder pain yes or no?
Time Frame
1, 8, 24, and 72 hours after surgery
Title
Post-operative nausea and vomiting (PONV)
Description
NRS 0-10
Time Frame
1, 8, 24 and 72 hours after surgery
Title
Cumulative use of analgesics and anti-emetics
Description
Total dose of opiates, other analgesics and anti-emetic drugs
Time Frame
1, 8, 24 and 72 hours after surgery
Title
Length of hospital stay
Description
Total number of days from admission to discharge after surgery (not including readmission)
Time Frame
From date of admission until date of discharge from the hospital (usually several days), assessed up to 3 months.
Title
Surgical conditions
Description
Rating of the surgical conditions with the Leiden Surgical Rating Scale (L-SRS). The L-SRS is scored by the surgeon and ranges from 1-5 for quality of the surgical field. A score of 5 means optimal conditions: a wide laparoscopic field with no patient movements or muscle contractions, 1 means extremely poor conditions: the surgeon is unable to obtain a visible laparoscopic field because of inadequate muscle relaxation.
Time Frame
Intraoperative: after introduction of the trocars and every 15 minutes until the end of the pneumoperitoneum.
Title
Intraoperative complications
Description
Complications during surgery graded according to the Clavien-Dindo classification
Time Frame
During surgery
Title
Postoperative complications
Description
Postoperative complications
Time Frame
Up to 3 months after surgery
Title
Time to reach discharge criteria
Description
Number of days to reach the following criteria after surgery: adequate pain control with oral medication, passage of flatus or defecation, intake of solid food tolerated, patient is mobilized and independent and patient accepts discharge.
Time Frame
From date of surgery until date of actual discharge from the hospital (usually several days), assessed up to 3 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Scheduled for laparoscopic colorectal surgery with a primary anastomosis Obtained informed consent Age over 18 years Exclusion Criteria: Insufficient control of the Dutch language to read the patient information and to fill out the questionnaires Primary colostomy Neo-adjuvant chemotherapy Chronic use of analgesics or psychotropic drugs Use of NSAIDs shorter than 5 days before surgery Known or suspected allergy to rocuronium of sugammadex Neuromuscular disease Indication for rapid sequence induction Severe liver- or renal disease (creatinine clearance <30ml/min) BMI >35 kg/m² Deficiency of vitamin K dependent clotting factors or coagulopathy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kim I Albers, MD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michiel C Warlé, MD, PhD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Canisius Wilhelmina Hospital
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6532SZ
Country
Netherlands
Facility Name
Martini general hospital
City
Groningen
Country
Netherlands
Facility Name
Maxima Medisch Centrum
City
Veldhoven
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32552782
Citation
Albers KI, Polat F, Panhuizen IF, Snoeck MMJ, Scheffer GJ, de Boer HD, Warle MC. The effect of low- versus normal-pressure pneumoperitoneum during laparoscopic colorectal surgery on the early quality of recovery with perioperative care according to the enhanced recovery principles (RECOVER): study protocol for a randomized controlled study. Trials. 2020 Jun 17;21(1):541. doi: 10.1186/s13063-020-04496-8.
Results Reference
derived

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The Effect of Low Pressure Pneumoperitoneum During Laparoscopic Colorectal Surgery on Early Quality of Recovery

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