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Diaphragm Ultrasound to Evaluate the Antagonistic Effect of Sugammadex

Primary Purpose

Diaphragm Ultrasonography, Liver Dysfunction, Sugammadex

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
sugammadex
Sponsored by
Wuhan Union Hospital, China
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Diaphragm Ultrasonography

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1.Age between 18 and 65 years old.
  • 2.Patients scheduled for laparoscopic radical resection of liver cancer under general anesthesia.
  • 3.Patients ASA classification Ⅰ-Ⅲ.
  • 4.Body mass index 18.5 kg/m2 ~ 24.9 kg/m2
  • 5.Able to give informed consent.
  • 6.The surgical position is suitable for BIS monitoring and muscle relaxation monitoring.

Exclusion Criteria:

  • 1.Patients with allergic to rocuronium and SUG.
  • 2.Patients with central and peripheral nervous system diseases, such as polio, Parkinson's disease, peripheral neuropathy, etc..
  • 3.Patients with neuromuscular system diseases, such as multiple sclerosis, myasthenia gravis, atrophic myotonia, etc..
  • 4.Patients with diaphragm dysfunction, pneumothorax, pleural effusion, mediastinal pneumatosis.
  • 5.Pregnant women or nursing mothers.
  • 6.Judging by the researchers, patients with other conditions who are unsuitable for clinical trials.

Sites / Locations

  • Union Hospital of Tongji Medical College of Huazhong University of Science and TechnologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Child-Pugh A

Child-Pugh B

Child-Pugh C

Arm Description

Diaphragm ultrasound scan before induction of anesthesia. Anesthesia method: During anesthesia induction, propofol 2.5mg/kg and sufentanil 5μg/kg will be injected intravenously. When the BIS value drops below 60, the muscle relaxation monitor will be calibrated. After T1 and TOF are stable, rocuronium will be injected intravenously at 0.6 mg/kg. During the maintenance stage of anesthesia, the pneumoperitoneum pressure will be at a low level of 8-10mmHg, propofol TCI will be applied to maintain the plasma concentration of 2.5-5.5 μg/mL, remifentanil TCI will be used to keep the plasma concentration of 0.5-5 ng/mL, and rocuronium will be continuously pumped intravenously with 0.3-0.6 mg/kg/h for deep muscle relaxations, with the the post-tetanic twitch count (PTC) value of 1 to 2. When the TOF value was ≥2%, patients in each group will be given SUG (2mg/kg). Diaphragm ultrasound scan at the immediate time,10min, 30min and 2h after extubation.

Diaphragm ultrasound scan before induction of anesthesia. Anesthesia method: During anesthesia induction, propofol 2.5mg/kg and sufentanil 5μg/kg will be injected intravenously. When the BIS value drops below 60, the muscle relaxation monitor will be calibrated. After T1 and TOF are stable, rocuronium will be injected intravenously at 0.6 mg/kg. During the maintenance stage of anesthesia, the pneumoperitoneum pressure will be at a low level of 8-10mmHg, propofol TCI will be applied to maintain the plasma concentration of 2.5-5.5 μg/mL, remifentanil TCI will be used to keep the plasma concentration of 0.5-5 ng/mL, and rocuronium will be continuously pumped intravenously with 0.3-0.6 mg/kg/h for deep muscle relaxations, with the the post-tetanic twitch count (PTC) value of 1 to 2. When the TOF value was ≥2%, patients in each group will be given SUG (2mg/kg). Diaphragm ultrasound scan at the immediate time,10min, 30min and 2h after extubation.

Diaphragm ultrasound scan before induction of anesthesia. Anesthesia method: During anesthesia induction, propofol 2.5mg/kg and sufentanil 5μg/kg will be injected intravenously. When the BIS value drops below 60, the muscle relaxation monitor will be calibrated. After T1 and TOF are stable, rocuronium will be injected intravenously at 0.6 mg/kg. During the maintenance stage of anesthesia, the pneumoperitoneum pressure will be at a low level of 8-10mmHg, propofol TCI will be applied to maintain the plasma concentration of 2.5-5.5 μg/mL, remifentanil TCI will be used to keep the plasma concentration of 0.5-5 ng/mL, and rocuronium will be continuously pumped intravenously with 0.3-0.6 mg/kg/h for deep muscle relaxations, with the the post-tetanic twitch count (PTC) value of 1 to 2. When the TOF value was ≥2%, patients in each group will be given SUG (2mg/kg). Diaphragm ultrasound scan at the immediate time,10min, 30min and 2h after extubation.

Outcomes

Primary Outcome Measures

the recovery rate of muscle relaxation
the incidence of residual muscle relaxation at different time points after the operation and the baseline recovery rate of the diaphragm(immediately after extubation, 10minutes, 30minutes and 2hours) When the patients' consciousness and spontaneous breathing are restored, participants can open their eyes according to the doctor's instructions, shake hands firmly, and at the same time, participants can complete the movement of raising their head continuously for more than 5 seconds to remove the tracheal tube.

Secondary Outcome Measures

muscle relaxation onset time
the period from administration of rocuronium to tracheal intubation
intraoperative rocuronium dosage
The sum of the dose of rocuronium bromide used in induction and maintenance of anesthesia.
PACU monitoring time
Total time patients are monitored in PACU after surgery.
the incidence of postoperative pulmonary complications
incidence of postoperative pulmonary complications within seven days

Full Information

First Posted
July 18, 2021
Last Updated
August 30, 2021
Sponsor
Wuhan Union Hospital, China
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1. Study Identification

Unique Protocol Identification Number
NCT05028088
Brief Title
Diaphragm Ultrasound to Evaluate the Antagonistic Effect of Sugammadex
Official Title
Diaphragm Ultrasound to Evaluate the Antagonistic Effect of Sugammadex on Rocuronium After Liver Surgery in Patients With Different Liver Child-Pugh Grades
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
July 1, 2021 (Actual)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wuhan Union Hospital, China

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The use of muscle relaxants is an indispensable in the general anesthesia but is prone to accidents, which are often related to residual muscle relaxant. Therefore, how to timely and effectively eliminate the residual effect of muscle relaxants after surgery has become an urgent clinical problem. Rocuronium is a non-depolarizing muscle relaxant that is primarily metabolized by the liver. Patients with liver dysfunction can affect the metabolic process of rocuronium, thereby delaying the recovery of muscle relaxation. Sugammadex (SUG) is a novel specific antagonist of aminosteroid muscle relaxants, which can effectively antagonize muscle relaxants at different depths. However, whether liver dysfunction affects the antagonistic effect of SUG against rocuronium has not been reported yet. Therefore, the investigators hypothesize that with the increase of patients' liver Child-Pugh grade, the recovery time of rocuronium antagonized by the same dose of SUG after surgery will be prolonged, and the incidence of muscle relaxation residual will be increased in the short term.
Detailed Description
Main instruments: Drager Fabius anesthesia machine, interlive vue MX600 monitor, Train-Of-Four-Watch muscle relaxation monitor, Philips IU22 Color Doppler Ultrasound Diagnostic Instrument. Diaphragm ultrasound scan: Prior to anesthesia induction, patients will lie on the bed in a semi-recumbent (45°) position. One operator skilled in ultrasonography will identify and locate diaphragm using the hyperechoic pleural and peritoneal layers with an Philips IU22 Color Doppler Ultrasound Diagnostic Instrument. Anesthesia method: After the patient entered the operating room, venous access will be opened in the forearm, and routine monitoring of non-invasive BP, ECG, oxygen saturation(SpO₂) and bispectral index(BIS) will be performed. During anesthesia induction, propofol 2.5mg/kg and sufentanil 5μg/kg will be injected intravenously. When the BIS value drops below 60, the muscle relaxation monitor will be calibrated. After T1 and TOF are stable, rocuronium will be injected intravenously at 0.6 mg/kg. By the time T1=0, endotracheal intubation will be given, and the respiratory parameters will need to be adjusted to volume control ventilation (VT 8-10 ml/kg, respiratory rate(RR) 12-18 times/min, and PETCO2 35-45 mmHg). During the maintenance stage of anesthesia, the pneumoperitoneum pressure will be at a low level of 8-10mmHg, propofol target-controlled infusion(TCI) will be applied to maintain the plasma concentration of 2.5-5.5 μg/mL, remifentanil TCI will be used to keep the plasma concentration of 0.5-5 ng/mL, and rocuronium will be continuously pumped intravenously with 0.3-0.6 mg/kg/h for deep muscle relaxations, with the the post-tetanic twitch count (PTC) value of 1 to 2. Muscle relaxation monitoring: TOF-Watch SX muscle relaxation monitor is going to be adopted in our study. The investigators will standardize the electrode position of the muscle relaxation monitor. The distal electrode will be placed at the intersection of the radial edge of the ulnar flexor carpi and the proximal edge of the wrist curve, while the proximal electrode will be placed 3-6 cm away from the distal electrode. Two electrodes will put on either side of the predicted location of the ulnar nerve, which will be able to minimize the impact caused by misjudgment of the location of the nerve. Measurement of diaphragmatic thickness: When B-mode ultrasound will be used to measure the thickness of the diaphragm, a 5-12MHz linear array ultrasound probe will be put in the left midaxillary line between the 8-10 costale, where is called the diaphragmatic zone of apposition (ZAP). In the breathing exercise, the diaphragm is relatively fixed at ZAP, and the breathing action has little influence on the movement of the diaphragm at ZAP, the diaphragm only shows systolic and diastolic changes. Therefore, the measurement of the diaphragm thickness at ZAP can truly reflect the overall thickness change of the diaphragm during the respiratory cycle. Each value will be measured three times in three consecutive breathing cycles, and the average of the nine measurements will be taken. The values of diaphragmatic thickness at the end of inspirations (DTEI) and diaphragmatic thickness at the end of expirations (DTEE) will be recorded respectively, then the change rate of diaphragmatic thickness fraction (DTF) = (DTEI - DTEE) / DTEE × 100% will be calculated. In addition, the recover rate of DTF = (pre-anesthetic DTEI - postoperative DTEI) / pre-anesthetic DTEI × 100% also will be figured out. Ultrasound measurements should be performed by two physicians with ultrasound experience. Results will be kept confidential to the investigator, who will analyze the ultrasound data when the research is over. The infusion of anesthetic drugs should be stopped at the end of surgery, and the patients will be transferred into the Post-Anesthesia Care Unit (PACU) with endotracheal catheters and continued monitoring. When the TOF value was ≥2%, patients in each group will be given SUG (2mg/kg), respectively. The researchers will record the recovery conditions of diaphragmatic function monitored by bedside ultrasound at the immediate time,10min, 30min and 2h after extubation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diaphragm Ultrasonography, Liver Dysfunction, Sugammadex, Rocuronium

7. Study Design

Primary Purpose
Other
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Non-Randomized
Enrollment
99 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Child-Pugh A
Arm Type
Experimental
Arm Description
Diaphragm ultrasound scan before induction of anesthesia. Anesthesia method: During anesthesia induction, propofol 2.5mg/kg and sufentanil 5μg/kg will be injected intravenously. When the BIS value drops below 60, the muscle relaxation monitor will be calibrated. After T1 and TOF are stable, rocuronium will be injected intravenously at 0.6 mg/kg. During the maintenance stage of anesthesia, the pneumoperitoneum pressure will be at a low level of 8-10mmHg, propofol TCI will be applied to maintain the plasma concentration of 2.5-5.5 μg/mL, remifentanil TCI will be used to keep the plasma concentration of 0.5-5 ng/mL, and rocuronium will be continuously pumped intravenously with 0.3-0.6 mg/kg/h for deep muscle relaxations, with the the post-tetanic twitch count (PTC) value of 1 to 2. When the TOF value was ≥2%, patients in each group will be given SUG (2mg/kg). Diaphragm ultrasound scan at the immediate time,10min, 30min and 2h after extubation.
Arm Title
Child-Pugh B
Arm Type
Experimental
Arm Description
Diaphragm ultrasound scan before induction of anesthesia. Anesthesia method: During anesthesia induction, propofol 2.5mg/kg and sufentanil 5μg/kg will be injected intravenously. When the BIS value drops below 60, the muscle relaxation monitor will be calibrated. After T1 and TOF are stable, rocuronium will be injected intravenously at 0.6 mg/kg. During the maintenance stage of anesthesia, the pneumoperitoneum pressure will be at a low level of 8-10mmHg, propofol TCI will be applied to maintain the plasma concentration of 2.5-5.5 μg/mL, remifentanil TCI will be used to keep the plasma concentration of 0.5-5 ng/mL, and rocuronium will be continuously pumped intravenously with 0.3-0.6 mg/kg/h for deep muscle relaxations, with the the post-tetanic twitch count (PTC) value of 1 to 2. When the TOF value was ≥2%, patients in each group will be given SUG (2mg/kg). Diaphragm ultrasound scan at the immediate time,10min, 30min and 2h after extubation.
Arm Title
Child-Pugh C
Arm Type
Experimental
Arm Description
Diaphragm ultrasound scan before induction of anesthesia. Anesthesia method: During anesthesia induction, propofol 2.5mg/kg and sufentanil 5μg/kg will be injected intravenously. When the BIS value drops below 60, the muscle relaxation monitor will be calibrated. After T1 and TOF are stable, rocuronium will be injected intravenously at 0.6 mg/kg. During the maintenance stage of anesthesia, the pneumoperitoneum pressure will be at a low level of 8-10mmHg, propofol TCI will be applied to maintain the plasma concentration of 2.5-5.5 μg/mL, remifentanil TCI will be used to keep the plasma concentration of 0.5-5 ng/mL, and rocuronium will be continuously pumped intravenously with 0.3-0.6 mg/kg/h for deep muscle relaxations, with the the post-tetanic twitch count (PTC) value of 1 to 2. When the TOF value was ≥2%, patients in each group will be given SUG (2mg/kg). Diaphragm ultrasound scan at the immediate time,10min, 30min and 2h after extubation.
Intervention Type
Drug
Intervention Name(s)
sugammadex
Other Intervention Name(s)
diaphragm ultrasonography
Intervention Description
This study is a prospective, double-blind, low-intervention, non-randomized controlled clinical trial involving 99 patients with American Society of Anesthesiologists Ⅰ-Ⅲ, body mass index 18.5-24.9 kg/m2, who will undergo laparoscopic radical resection of liver cancer under general anesthesia in the Wuhan Union Hospital. Ultrasonography will be applied to monitor the change rate of diaphragm thickness at different time after extubation to evaluate the recovery rate of muscle relaxant, which indirectly reflects the dose-effect relationship of SUG antagonizing against rocuronium in patients with different liver Child-Pugh grades preoperatively.
Primary Outcome Measure Information:
Title
the recovery rate of muscle relaxation
Description
the incidence of residual muscle relaxation at different time points after the operation and the baseline recovery rate of the diaphragm(immediately after extubation, 10minutes, 30minutes and 2hours) When the patients' consciousness and spontaneous breathing are restored, participants can open their eyes according to the doctor's instructions, shake hands firmly, and at the same time, participants can complete the movement of raising their head continuously for more than 5 seconds to remove the tracheal tube.
Time Frame
2 hours
Secondary Outcome Measure Information:
Title
muscle relaxation onset time
Description
the period from administration of rocuronium to tracheal intubation
Time Frame
within 3 minutes
Title
intraoperative rocuronium dosage
Description
The sum of the dose of rocuronium bromide used in induction and maintenance of anesthesia.
Time Frame
through anesthesia completion, up to 2 hours
Title
PACU monitoring time
Description
Total time patients are monitored in PACU after surgery.
Time Frame
about 2 hours
Title
the incidence of postoperative pulmonary complications
Description
incidence of postoperative pulmonary complications within seven days
Time Frame
within 7 days after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1.Age between 18 and 65 years old. 2.Patients scheduled for laparoscopic radical resection of liver cancer under general anesthesia. 3.Patients ASA classification Ⅰ-Ⅲ. 4.Body mass index 18.5 kg/m2 ~ 24.9 kg/m2 5.Able to give informed consent. 6.The surgical position is suitable for BIS monitoring and muscle relaxation monitoring. Exclusion Criteria: 1.Patients with allergic to rocuronium and SUG. 2.Patients with central and peripheral nervous system diseases, such as polio, Parkinson's disease, peripheral neuropathy, etc.. 3.Patients with neuromuscular system diseases, such as multiple sclerosis, myasthenia gravis, atrophic myotonia, etc.. 4.Patients with diaphragm dysfunction, pneumothorax, pleural effusion, mediastinal pneumatosis. 5.Pregnant women or nursing mothers. 6.Judging by the researchers, patients with other conditions who are unsuitable for clinical trials.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yun Lin, MD, PhD.
Phone
+86 02785351606
Email
franklinyun@hust.edu.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Shujun Sun
Phone
15804066597
Email
sunshunjun@foxmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yun Lin, MD, PhD.
Organizational Affiliation
Union Hospital of Tongji Medical College of Huazhong University of Science and Technology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Union Hospital of Tongji Medical College of Huazhong University of Science and Technology
City
Wuhan
State/Province
Hubei
ZIP/Postal Code
430022
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yun Lin, MD, PhD.
Phone
+86 02785351606
Email
franklinyun@hust.edu.cn
First Name & Middle Initial & Last Name & Degree
Shujun Sun
Phone
+86 02785351606
Email
sunshunjun@foxmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The investigators don not plan to make the IPD collected in this study available to other researchers.
Citations:
PubMed Identifier
1718602
Citation
Whittaker R, Wedell D. Review of neuromuscular blockers. Compendium. 1991 Jun;12(6):408, 410, 412 passim.
Results Reference
background
PubMed Identifier
9512917
Citation
Naguib M, Magboul MM. Adverse effects of neuromuscular blockers and their antagonists. Drug Saf. 1998 Feb;18(2):99-116. doi: 10.2165/00002018-199818020-00002.
Results Reference
background
PubMed Identifier
20422848
Citation
Arino-Irujo JJ, Calbet-Manueco A, De la Calle-Elguezabal PA, Velasco-Barrio JM, Lopez-Timoneda F, Ortiz-Gomez JR, Fabregat-Lopez J, Palacio-Abizanda FJ, Fornet-Ruiz I, Perez-Cajaraville J. [Neuromuscular blockade monitoring. Part 1]. Rev Esp Anestesiol Reanim. 2010 Mar;57(3):153-60. doi: 10.1016/s0034-9356(10)70190-0. Spanish.
Results Reference
background
PubMed Identifier
28573344
Citation
Fuchs-Buder T, Schmartz D. [Residual neuromuscular blockade]. Anaesthesist. 2017 Jun;66(6):465-476. doi: 10.1007/s00101-017-0325-1. Erratum In: Anaesthesist. 2017 Aug;66(8):578. German.
Results Reference
background
PubMed Identifier
27820709
Citation
Brull SJ, Kopman AF. Current Status of Neuromuscular Reversal and Monitoring: Challenges and Opportunities. Anesthesiology. 2017 Jan;126(1):173-190. doi: 10.1097/ALN.0000000000001409.
Results Reference
background
PubMed Identifier
20442260
Citation
Murphy GS, Brull SJ. Residual neuromuscular block: lessons unlearned. Part I: definitions, incidence, and adverse physiologic effects of residual neuromuscular block. Anesth Analg. 2010 Jul;111(1):120-8. doi: 10.1213/ANE.0b013e3181da832d. Epub 2010 May 4.
Results Reference
background
PubMed Identifier
26768931
Citation
Aytac I, Postaci A, Aytac B, Sacan O, Alay GH, Celik B, Kahveci K, Dikmen B. Survey of postoperative residual curarization, acute respiratory events and approach of anesthesiologists. Braz J Anesthesiol. 2016 Jan-Feb;66(1):55-62. doi: 10.1016/j.bjane.2012.06.011. Epub 2014 Apr 4.
Results Reference
background
PubMed Identifier
32416089
Citation
Shay D, Wongtangman K, Eikermann M, Schaefer MS. The effects of acetylcholinesterase inhibitors on morbidity after general anesthesia and surgery. Neuropharmacology. 2020 Aug 15;173:108134. doi: 10.1016/j.neuropharm.2020.108134. Epub 2020 May 19.
Results Reference
background
PubMed Identifier
31272347
Citation
Hawkins J, Khanna S, Argalious M. Sugammadex for Reversal of Neuromuscular Blockade: Uses and Limitations. Curr Pharm Des. 2019;25(19):2140-2148. doi: 10.2174/1381612825666190704101145.
Results Reference
background
PubMed Identifier
31558731
Citation
Tao J, Zhang W, Yue H, Zhu G, Wu W, Gong W, Fang H, He G, Hu X, Zhao H, Liu A. Prevalence of Hepatitis B Virus Infection in Shenzhen, China, 2015-2018. Sci Rep. 2019 Sep 26;9(1):13948. doi: 10.1038/s41598-019-50173-5.
Results Reference
background
PubMed Identifier
35105573
Citation
Sun S, Sun Y, Chen R, Yao C, Xia H, Chen X, Lin Y, Yao S. Diaphragm ultrasound to evaluate the antagonistic effect of sugammadex on rocuronium after liver surgery in patients with different liver Child-Pugh grades: study protocol for a prospective, double-blind, non-randomised controlled trial. BMJ Open. 2022 Feb 1;12(2):e052279. doi: 10.1136/bmjopen-2021-052279.
Results Reference
derived

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Diaphragm Ultrasound to Evaluate the Antagonistic Effect of Sugammadex

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