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Completed

NCT Number: NCT04250883

Low Pressure Pneumoperitoneum and Deep Neuromuscular Block vs. Standard During RARP to Improve Quality of Recovery; a Randomized Controlled Study.

Intra-abdominal pressure (IAP) needed to create sufficient workspace during laparoscopic surgery affects the surrounding organs with ischemia-reperfusion injury and a systemic immune response. This effect is related to postoperative recovery, pain scores, opioid consumption, bowel function recovery, morbidity and possibly mortality. In clinical practice standard pressures of 12-16mmHg are applied instead of the lowest possible IAP, but accumulating evidence shows lower pressure pneumoperitoneum (PNP) (6-8mmHg) to be non-compromising for sufficient workspace, when combined with deep neuromuscular blockade (NMB) in a vast majority of patients. Therefore, low impact laparoscopy, meaning low pressure PNP facilitated by deep NMB, could be a valuable addition to Enhanced Recovery After Surgery (ERAS) Protocols.

The use of low pressure PNP may also reduce hypoxic injury and the release of DAMPs and thereby contributing to a better preservation of innate immune function which may help to reduce the risk of infectious complications.

The participants will be randomly assigned to one of the experimental groups with low impact laparoscopy or one of the control groups with standard laparoscopy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Canisius Wilhelmina ziekenhuis

Nijmegen, Netherlands

About this study

Intra-abdominal pressure (IAP) needed to create sufficient workspace during laparoscopic surgery affects the surrounding organs with ischemia-reperfusion injury and a systemic immune response. This effect is related to postoperative recovery, pain scores, opioid consumption, bowel function recovery, morbidity and possibly mortality. Therefore, low impact laparoscopy, meaning low pressure PNP facilitated by deep NMB, could be a valuable addition to Enhanced Recovery After Surgery (ERAS) Protocols.

The use of low pressure PNP may also reduce hypoxic injury and the release of DAMPs and thereby contributing to a better preservation of innate immune function which may help to reduce the risk of infectious complications.

The participants will be randomly assigned to the experimental group 1: low impact laparoscopy (low pressure (8 mmHg) and deep NMB (PTC 1-2)); 8 mmHg IAP after trocar introduction for perfusion measurement or the experimental group 2: low impact laparoscopy (low pressure (8 mmHg) and deep NMB (PTC 1-2)); 12 mmHg IAP after trocar introduction for perfusion measurement, or control group 1: standard laparoscopy (standard pressure (12 mmHg) and moderate NMB (TOF 1-2)); 8 mmHg IAP after trocar introduction for perfusion measurement, or control group 2: standard laparoscopy (standard pressure (12 mmHg) and moderate NMB (TOF 1-2)); 12 mmHg IAP after trocar introduction for perfusion measurement.

ICG injection will take place with starting pressure to quantify parietal peritoneum perfusion, and a parietal peritoneal biopsy will be taken. At the end of surgery, a second parietal peritoneum biopsy will be taken.

NB: After introduction of the camera trocar, insufflation of carbon dioxide is titrated to an IAP of 8mmHg in group A and C, and 14 mmHg in group B and D. After placement of the last trocar the injection of ICG and video registration of peritoneum will take place, and a peritoneal biopsy will be taken. There after surgery will take place with an IAP of 14mmHg in the control groups (C and D), and an IAP of 8mmHg in the experimental groups (A and B). In the control groups (C and D)

Pre- and postoperative a few questionnaires will be taken and blood withdrawals to evaluate the quality of recovery, and the immune response.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • - Age ≥ 18 years
  • Undergoing elective robot assisted radical prostatectomy (RARP)
  • Obtained informed consent

Exclusion criteria

  • Laparoscopic radical prostatectomy without robot assistance
  • Insufficient control of the Dutch language to read the patient information and to fill out de questionnaires
  • Neo-adjuvant chemotherapy
  • Chronic use of analgesics or psychotropic drugs
  • Use of NSAID's shorter than 5 days before surgery
  • Severe liver- or renal disease
  • Neuromuscular disease
  • Hyperthyroidism or thyroid adenomas
  • Deficiency of vitamin K dependent clotting factors or coagulopathy
  • Planned diagnostics or treatment with radioactive iodine < 1 week after surgery
  • Indication for rapid sequence induction
  • BMI >35kg/m2
  • Known of suspected hypersensitivity to ICG, sodium iodide, iodine, rocuronium or sugammadex
  • Use of medication interfering with ICG absorption as listed in the summary of product characteristics (SPC); anticonvulsants, bisulphite compounds, haloperidol, heroin, meperidine, metamizol, methadone, morphium, nitrofurantoin, opium alkaloids, phenobarbital, phenylbutazone, cyclopropane, probencid

Treatment and study plan

Low intra-abdominal pressure

Other

8 mmHg

Deep neuromuscular blockade (NMB)

Other

Deep NMB (PTC1-2)

Standard intra-abdominal pressure

Other

14 mmHg

Moderate neuromuscular blockade (NMB)

Other

Moderate NMB (TOF 1-2)

Primary outcomes

  1. Quality of Recovery - 40 Items Questionnaire Score (QoR-40)

    Time frame: at postoperative day 1

    40 points (minimum: extremely poor quality of recovery) to 200 points (maximum: excellent quality of recovery)

  2. Quality of Recovery - 40 Items Questionnaire Score (QoR-40)

    Time frame: day 12 after surgery

    40 points (minimum: extremely poor quality of recovery) to 200 points (maximum: excellent quality of recovery)

  3. Quality of Recovery - 40 Items Questionnaire Score (QoR-40)

    Time frame: Pre-operative

    40 points (minimum: extremely poor quality of recovery) to 200 points (maximum: excellent quality of recovery)

Secondary outcomes

  1. Health Status With Short Form Survey (SF-36)

    Time frame: Measure pre-operative, on day 12 and at 3 months after surgery

    Total score on a scale of 0-100 points. The lower the score the more disability. The higher the score the less disability.

  2. Chronic Pain With McGill Pain Questionnaire (MPQ)

    Time frame: 3 months after surgery

    Pain Rating index with a range from 0 (no pain) to 78 (severe pain)

  3. Operating Conditions

    Time frame: During operation for up to 8 hours

    surgical conditions with L-SRS 0 (extremely poor work field) to 5 (excellent work field)

  4. Pain Score With NRS

    Time frame: Preset timepoints during hospital stay (1hr, 6hrs, 12hrs, day1), up to 3 days maximum. No measurements after discharge to home.

    pain scores with NRS 0 (no pain) to 10 (severe pain)

  5. Postoperative Nausea and Vomiting (PONV)

    Time frame: During hospital stay up to 3 days

    Presence of symptoms yes/no

  6. Analgesia Use

    Time frame: During hospital stay up to 3 days

    Cumulative opioid use in morphine equivalent (in mg)

  7. Hospital Stay

    Time frame: from admission up to 3 days

    length of hospital stay in days

  8. Complications

    Time frame: Day of surgery untill 30days after surgery

    Postoperative complications scored by Clavien Dindo classification; grade 0 (no deviation from ideal) grade 5 (death of patient)

  9. Perfusion Index of the Parietal Peritoneum

    Time frame: From ICG injection, up to 20 seconds

    time to maximal intensity in seconds. (extracted from video registration).

  10. Immune Response Represented by IL-10

    Time frame: Pre-operative, postoperative day 1 and 12

    IL-10 response upon whole blood LPS stimulation

  11. Immune Response Represented by IL-6

    Time frame: Pre-operative, postoperative day 1 and 12

    IL-6 response upon whole blood LPS stimulation

  12. Chronic Pain With McGill Pain Questionnaire (MPQ)

    Time frame: 3 months after surgery

    Number of words Chosen according the user manual of the questionnaire

  13. Perfusion Index of the Parietal Peritoneum

    Time frame: From ICG injection, up to 20 seconds

    Angle minimal to maximal, calculated from the slope of ICG fluorescence intensity (extracted from video registration).

Other outcomes

  1. Duration of Surgery

    Time frame: 0-350minutes

    in minutes

  2. Duration of Pneumoperitoneum

    Time frame: 0-350 minutes

    in minutes

  3. Estimated Blood Loss

    Time frame: During operation

    during operation time in ml

Sponsors and collaborators

Lead sponsor

Radboud University Medical Center

Other

Collaborators

  • Merck Sharp & Dohme LLC

Registry information

Official study title

Low Pressure Pneumoperitoneum and Deep Neuromuscular Blockade Versus Standard Laparoscopy During RARP to Improve the Quality of Recovery and Immune Homeostasis; Study Protocol for a Randomized Controlled Study

Acronym: RECOVER-2

Important dates

Study start
2020
Primary completion
2021
Study completion
2022
First posted
Jan 31, 2020
Registry last updated
Feb 5, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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