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Does Depth of Neuromuscular Blockade (NMB) Affect Surgical Conditions in Obese Patients Undergoing Robotic Surgery (NMB)

Primary Purpose

GYN Disorders, Urologic Diseases

Status
Withdrawn
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
NMB with rocuronium bromide
Sponsored by
Rainer Lenhardt
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for GYN Disorders focused on measuring Robotic Surgery

Eligibility Criteria

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

Inclusion Criteria:

  1. Patients scheduled for elective robotic gynecological or urologic surgery under general anesthesia.
  2. Patients are willing and sign an IRB approved consent
  3. Patients will be 18 years or older

Exclusion Criteria:

  1. Patients with atrial fibrillation
  2. Other significant arrhythmia (Lown grade 3 or greater)
  3. Patients with aortic regurgitation
  4. Unable to receive or refuses to usehydromorphone for pain management post-operatively (allergic, bad experience previously with use)

Sites / Locations

  • University of Louisville Medical School, Department of Anesthesiology and Perioperative Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Deep NMB

Moderate NMB

Arm Description

Deep NMB: Intervention: Rocuronium will be given as a continuous infusion for deep block. TOF will be maintained at 0 (zero) with at least one PTC. Patients' paralysis will be continued through the anesthesia period. At the end of surgery, patients will receive 4 mg/kg sugammadex and the patient's trachea will be extubated according to routine extubation criteria.

Moderate NMB: Intervention: Rocuronium will be used as bolus doses to achieve a moderate block. TOF will be maintained between 1 to 3 twitches. PTC will not be counted. Paralysis will be continued throughout the anesthesia period. At the end of surgery, patients will receive 2 mg/kg sugammadex and the patient's trachea will be extubated according to routine extubation criteria.

Outcomes

Primary Outcome Measures

Assessment of surgical conditions during deep versus moderate NMB in patients undergoing robotic abdominal surgery
Surgical conditions will be assessed by the Leiden surgical rating scale (Martini BJA 2014; 112:498) as follows: Scale range from 1 to 5 with 1 describing extremely poor conditions and 5 describing optimal conditions for surgery

Secondary Outcome Measures

Assessment of PVI changes to predict fluid responsiveness in robotic surgery
PVI changes will be measured after each fluid challenge and correlated with a change in stroke volume
Incidence of good and optimal surgical conditions in obese and non-obese patients undergoing robotic abdominal surgery
Surgical conditions will be assessed by the Leiden surgical rating scale and will be compared in obese patients versus non-obese patients Surgical conditions will be assessed by the Leiden surgical rating scale (Martini BJA 2014; 112:498) as follows: Scale range from 1 to 5 with 1 describing extremely poor conditions and 5 describing optimal conditions for surgery
Assessment of postoperative pain after deep versus moderate NMB in patients undergoing robotic abdominal surgery. Does depth of neuromuscular block (NMB) affect postoperative pain ?
Postoperative pain will be measured by visual pain analogue scale and by the amount of hydromorphone used in 24 hours after surgery. Pain assessments will be completed using the "visual pain analogue scale" (VAS). VAS scale ranges from 1 to 100 mm, with 1 meaning no pain at all to 100 rated as the worst pain imaginable

Full Information

First Posted
November 3, 2017
Last Updated
July 14, 2021
Sponsor
Rainer Lenhardt
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1. Study Identification

Unique Protocol Identification Number
NCT03591289
Brief Title
Does Depth of Neuromuscular Blockade (NMB) Affect Surgical Conditions in Obese Patients Undergoing Robotic Surgery
Acronym
NMB
Official Title
Does Depth of Neuromuscular Blockade (NMB) Affect Surgical Conditions and Postoperative Pain in Obese Patients Undergoing Robotic Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Withdrawn
Why Stopped
study never started up at site
Study Start Date
February 2018 (Anticipated)
Primary Completion Date
February 2018 (Anticipated)
Study Completion Date
July 12, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Rainer Lenhardt

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A prospective, randomized, outcome trial to evaluate, if depth of neuromuscular blockade (NMB) will affect surgical conditions and postoperative pain based on the degree of neuromuscular block during robotic surgery for gynecological and urologic procedures in obese and non-obese patients.
Detailed Description
Study Procedures: Anesthesia will be induced with propofol (2 mg/kg), fentanyl (1-2 µg/kg) and rocuronium (0.6 mg/kg) to facilitate intubation. A #8 endotracheal tube in males and #7endotracheal tube in females will be inserted in the trachea and secured at 22 cm. Anesthesia will be maintained with sevoflurane to maintain the BIS value between 40 and 60. Analgesia will be provided with fentanyl at 1-2 µg/kg/h or remifentanil 0.5-2 µg/kg/min. Anesthesia will continue until surgery is completed. Patients will be randomized to either deep neuromuscular blockade (NMB) or moderate NMB as described below. Rocuronium will be administered to keep NMB deep or moderate NMB according to the randomization. Deep NMB: Rocuronium will be given as a continuous infusion for deep block. Train of four (TOF) will be maintained at 0 (zero) with at least one post-tetanic count (PTC). Patients' paralysis will be continued through the anesthesia period. At the end of surgery, deep Block patients' will receive 4 mg/kg sugammadex and the patient's trachea will be extubated according to routine extubation criteria. Moderate NMB: Rocuronium will be used as bolus doses to achieve a moderate block. TOF will be maintained between 1 to 3 twitches. PTC will not be counted. Paralysis will be continued throughout the anesthesia period. At the end of surgery, patients will receive 2 mg/kg sugammadex in the moderate NMB and the patient's trachea will be extubated according to routine extubation criteria. NMB will be assessed by acceleromyography (STIMPOD NMS410 Peripheral Nerve Stimulator, Xavant Technology (Pty) Ltd. Silverton, Pretoria, South Africa) The ventilator will be set at pressure-controlled mode and patients will be ventilated with an airway pressure corresponding to a tidal volume of 8 mL/kg up to a maximum airway pressure of 35 cmH20. Inspired oxygen will be kept near 50% but will be increased if necessary to maintain a hemoglobin oxygen saturation ≥95%. PEEP will be set at 5 cmH20. Respiratory rate will be 12 breaths per minute. Patients' will have a small finger cuff (finger plethysmography) with a transducer and continuous real-time cardiovascular monitor (Edwards, Life Science, Irvine, CA) The patient may also receive an arterial catheter (radial artery) for continuous real-time cardiovascular monitoring based on the clinicians' preference. Arterial waveform will be recorded continuously. A pulse oximeter (LNOP Adt, Masimo Corp, Irvine, CA) will be attached to the index finger of the patient's same hand and connected to a bedside monitor (Radical 7, Masimo Corp, Irvine, CA); the oximeter will be wrapped to prevent interference from outside light. Perfusion variability index (PVI) calculates the respiratory variations in the plethysmography waveform amplitude (Perfusion index [PI]) using the maximum and minimum PI values over a given time period. Intraoperative fluid management will be performed with normosol 2 mL/kg/h. Fluid boluses will be given as guided by stroke volume variation (SVV). Hetastarch will be given as a bolus in 250 mL increments to a maximum of 50 mL/kg. The fluid bolus will be given over 2 minutes. A bladder (foley) catheter will be inserted after induction of anesthesia. This is part of conventional care and allows for more accurate fluid volume tracking. Once the patient is in Trendelenburg position and should a measurement yield that SVV is staying above 10%, a fluid bolus of 250 mL of hetastarch will be given over 2 minutes and repeated until the SVV falls below 10%. During abdominal CO2 insufflation, the intra-abdominal pressure will be kept at 15 cmH2O. The Trendelenburg position will be 30º, which corresponds to the maximum inclination of the OR table. Postoperatively, patients will receive a bilateral transverse abdominal plane (TAP) block with ropivacaine in the post-operative area. Patients will receive a PCA pump with hydromorphone for pain management.(This is all standard practice). Measurements: A) Measurements that will be recorded once the patient is brought into the operating room and throughout the intraoperative period include: 1. Hemodynamic data; Systolic, diastolic and mean arterial blood pressure in mmHg, Cardiac Output and Cardiac Index in liters per minute, Stroke Volume Variation in percent, Pulse Pressure Variation in percent, Perfusion Index (number from 0.1-10, no units), Perfusion Variability Index in percent Time points the data will be recorded include: After patients placement on operative table, while still awake, lying flat for one minute but prior to induction. Intraoperative, one minute after induction of anesthesia and intubation Intraoperative, one minute after initiation of pneumoperitoneum, with just one trocar placed Intraoperative, one minute after positioning the patient in Trendelenburg position but before the surgeon begins Intraoperative, every 15 minutes during the surgical procedure. Intraoperative, when the surgeon states the surgery is completed. Intraoperative, after surgery completed and one minute after reversal of Trendelenburg position. Intraoperative, while the patient is still on the operative table, one minute after deflation of the peritoneum. Intraoperative; additional measurements (as referred to above) may be recorded to capture observed changes that occurred during surgery. B) Measurements that will be recorded after general anesthesia has been induced and throughout the intraoperative period include (same time points as above minus time point one): 2. Assessment of NMB C) A 5-point surgical rating scale will be used to assess surgical conditions every 15 minutes: 1. The surgeon and the surgical assistant will be asked about surgical conditions every 15 minutes. Surgical conditions will be assessed by the Leiden surgical rating scale (Martini BJA 2014; 112:498). Extremely poor conditions: The surgeon is unable to work due to coughing or due to the inability to obtain a visible laparoscopic field because of inadequate muscle relaxation. Additional muscle relaxants must be given. Poor conditions: There is a visible laparoscopic field but the surgeon is severely hampered by inadequate muscle relaxation with continuous muscle contractions and/or movements with the hazard of tissue damage. Additional muscle relaxants must be given. Acceptable conditions: There is a wide visible laparoscopic field but muscle contractions and/or movements occur regularly causing some interference with the surgeon's work. There is the need for additional muscle relaxants to prevent deterioration. Good conditions: There is a wide laparoscopic working field with sporadic muscle contractions and/or movements. There is no immediate need for additional muscle relaxants unless there is the fear for deterioration. Optimal conditions: There is a wide visible laparoscopic working field without any movement or contractions. There is no need for additional muscle relaxants. 2. Intraoperatively; The Intra-abdominal pressures (mmHg) will be recorded every 15 minutes during the surgery. The amount of flow and the total amount of CO2 (in liters) will be recorded. 3. Forearm - fingertip temperature gradients will be measured by Mon-a-thermometer (Mallinckrodt Medical, Inc. St. Louis, MO) and disposable Mon-a-therm thermocouples. Vasoconstriction will be identified when forearm - fingertip temperature gradient is ≥ 00 Cº and PI < 1. D) Additional assessments: Intraoperatively; the surgical assistant will report any episode(s) of abdominal contractions throughout the surgery. The degree of the patients' Trendelenburg position will be measured intra-operatively with an angle ruler. The amount of rocuronium received intraoperatively, during the course of surgery, will be recorded. Subjects demographic information will be collected at the time of consent. This will include, age, gender, weight in kilograms, height in centimeters, BMI in kg/m^2, waist-to hip ratio, surgical procedure and co-morbidities. E) Post-operative assessments: Pain assessments will be completed using the "visual pain analogue scale" (VAS scale from 1 to 100 mm, with 1 meaning no pain at all to 100 rated as the worst pain imaginable). Assessments will be completed by a study team member. Patients will be asked about their pain level by visual analogue scale at the following time points: Baseline; in pre-operative holding area One hour after admission to PACU, post-operatively Six hours postoperatively Post-operative day one (next morning) between 0600 and 1000 Postoperative hydromorphone PCA requirement will be recorded up until the post-operative DAY ONE (Overall amount of hydromorphone measured in milligrams total). Pain assessment will be completed between 0600 and 1000 am. All other pain management (rescue) medications the patient received up to the time of the "AM" post-operative assessment will be recorded.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
GYN Disorders, Urologic Diseases
Keywords
Robotic Surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
two different regimens (doses) of two drugs (Rocuronium, Sugammadex)
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Subjects will not be informed to which NMB depth they were randomized to.
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Deep NMB
Arm Type
Active Comparator
Arm Description
Deep NMB: Intervention: Rocuronium will be given as a continuous infusion for deep block. TOF will be maintained at 0 (zero) with at least one PTC. Patients' paralysis will be continued through the anesthesia period. At the end of surgery, patients will receive 4 mg/kg sugammadex and the patient's trachea will be extubated according to routine extubation criteria.
Arm Title
Moderate NMB
Arm Type
Active Comparator
Arm Description
Moderate NMB: Intervention: Rocuronium will be used as bolus doses to achieve a moderate block. TOF will be maintained between 1 to 3 twitches. PTC will not be counted. Paralysis will be continued throughout the anesthesia period. At the end of surgery, patients will receive 2 mg/kg sugammadex and the patient's trachea will be extubated according to routine extubation criteria.
Intervention Type
Drug
Intervention Name(s)
NMB with rocuronium bromide
Other Intervention Name(s)
Reversal with suggammadex
Intervention Description
Moderate versus deep neuromuscular block Not a device study
Primary Outcome Measure Information:
Title
Assessment of surgical conditions during deep versus moderate NMB in patients undergoing robotic abdominal surgery
Description
Surgical conditions will be assessed by the Leiden surgical rating scale (Martini BJA 2014; 112:498) as follows: Scale range from 1 to 5 with 1 describing extremely poor conditions and 5 describing optimal conditions for surgery
Time Frame
data will be reported every 15 minutes starting post anesthesia induction until the end of general anesthesia
Secondary Outcome Measure Information:
Title
Assessment of PVI changes to predict fluid responsiveness in robotic surgery
Description
PVI changes will be measured after each fluid challenge and correlated with a change in stroke volume
Time Frame
PVI will be measured every 15 minutes and after any fluid bolus. Fluid bolus will be given, when PVI is > 12
Title
Incidence of good and optimal surgical conditions in obese and non-obese patients undergoing robotic abdominal surgery
Description
Surgical conditions will be assessed by the Leiden surgical rating scale and will be compared in obese patients versus non-obese patients Surgical conditions will be assessed by the Leiden surgical rating scale (Martini BJA 2014; 112:498) as follows: Scale range from 1 to 5 with 1 describing extremely poor conditions and 5 describing optimal conditions for surgery
Time Frame
Data will be reported every 15 minutes starting post anesthesia induction until the end of general anesthesia
Title
Assessment of postoperative pain after deep versus moderate NMB in patients undergoing robotic abdominal surgery. Does depth of neuromuscular block (NMB) affect postoperative pain ?
Description
Postoperative pain will be measured by visual pain analogue scale and by the amount of hydromorphone used in 24 hours after surgery. Pain assessments will be completed using the "visual pain analogue scale" (VAS). VAS scale ranges from 1 to 100 mm, with 1 meaning no pain at all to 100 rated as the worst pain imaginable
Time Frame
First 24 hours postoperatively at time points 1hour, 6 hours after surgery and postoperative day one

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients scheduled for elective robotic gynecological or urologic surgery under general anesthesia. Patients are willing and sign an IRB approved consent Patients will be 18 years or older Exclusion Criteria: Patients with atrial fibrillation Other significant arrhythmia (Lown grade 3 or greater) Patients with aortic regurgitation Unable to receive or refuses to usehydromorphone for pain management post-operatively (allergic, bad experience previously with use)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabeth Cooke, RN,BSN, CCRP
Organizational Affiliation
University of Louisville
Official's Role
Study Director
Facility Information:
Facility Name
University of Louisville Medical School, Department of Anesthesiology and Perioperative Medicine
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40202
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Does Depth of Neuromuscular Blockade (NMB) Affect Surgical Conditions in Obese Patients Undergoing Robotic Surgery

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