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Effects of Perioperative Transauricular Vagus Nerve Electrical Stimulation on POD, POCD and CPSP

Primary Purpose

Postoperative Cognitive Dysfunction, Postoperative Delirium, Chronic Post Operative Pain

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
transaricular vagus nerve stimulation
fake transaricular vagus nerve stimulation
Sponsored by
Xuzhou Central Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Postoperative Cognitive Dysfunction

Eligibility Criteria

50 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 50 to 80 years old.
  • ASA grade I-Ⅲ.
  • elective knee or hip replacement.

Exclusion Criteria:

  • Mini-Mental State Examination (MMSE) score < 23.
  • Education years<7.
  • Peptic ulcer disease, serious cardiac-cerebral vascular disease.
  • Neurological or psychiatric disorders.
  • History of drug and alcohol abuse.
  • Hepatic and/or kidney dysfunction.
  • BMI>35.
  • Patients on antidepressants.
  • ASA >Ⅲ.

Sites / Locations

  • Xuzhou Central Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Experimental group

Control group

Arm Description

The transaricular vagus nerve stimulator was placed in the left ear trunk, which is dominated only by the auricular branch of the vagus nerve. Continuous stimulation was performed at a frequency of 25Hz with pulse width of 300 μs. The stimulation was adjusted to be higher than the perception threshold and lower than the pain threshold. Each stimulation lasted for 30 minutes, three times per day (morning, noon, evening), from 1 day before surgery to 7 days after surgery, and the treatment lasted for 9 consecutive days.

The transaricular vagus nerve stimulator was placed in the same position as the experimental group, covered with an insulating film and placed at the site of the stimulation, so that the patient could not actually receive the electrical stimulation. Continuous stimulation was performed at a frequency of 25Hz and pulse width of 300 μs, and the stimulation was adjusted to be higher than the perception threshold and lower than the pain threshold. Each stimulation lasted for 30 minutes, three times per day (morning, noon, evening), from 1 day before surgery to 7 days after surgery, for 9 consecutive days.

Outcomes

Primary Outcome Measures

Postoperative cognitive function
The incidence of POCD was compared between the experimental group and the control group.The preoperative and postoperative differences of the following scales were calculated and compared: Digit Span (forward and backward), Visual Retention and Paired Associate Verbal Learning subtests of the Wechsler Memory Scale, Digit Symbol subtest of the Wechsler Adult Intelligence ScaleRevised, Halstead-Reitan Trail Making Test (Part A), Corsi Block Test and Grooved Pegboard Test (favored and unfavored hand). The standard deviation (SD) for each test was computed from the preoperative scores. A participant whose postoperative performance declined by ≥1 SD as compared to each preoperative test score on ≥2 tests was classified as POCD.
Postoperative cognitive function
The incidence of POCD was compared between the experimental group and the control group.The preoperative and postoperative differences of the following scales were calculated and compared: Digit Span (forward and backward), Visual Retention and Paired Associate Verbal Learning subtests of the Wechsler Memory Scale, Digit Symbol subtest of the Wechsler Adult Intelligence ScaleRevised, Halstead-Reitan Trail Making Test (Part A), Corsi Block Test and Grooved Pegboard Test (favored and unfavored hand). The standard deviation (SD) for each test was computed from the preoperative scores. A participant whose postoperative performance declined by ≥1 SD as compared to each preoperative test score on ≥2 tests was classified as POCD.
Postoperative delirium
The incidence of POD was compared between the experimental group and the control group.Postoperative delirium was assessed by the Delirium Assessment Scale (CAM-ICU)
Acute postoperative pain
The incidence of acute postoperative pain was compared between the experimental group and the control group.Acute postoperative pain was assessed by Visual Analogue Scale(VAS) for 7 consecutive days within 1 week after surgery.
Chronic Postsurgical pain
The incidence of chronic postoperative pain (CPSP) was assessed by the Short Form McGill Pain Questionnaire (SF-MPQ) and Neuropathic Pain Scale (NPS).The incidence of CPSP was compared between the experimental group and the control group.

Secondary Outcome Measures

TNF-α level in peripheral venous blood
The incidence of TNF-α level (pg/ml) in peripheral venous blood was compared between the experimental group and the control group
IL-6 level in peripheral venous blood
The incidence of IL-6 level (pg/ml) in peripheral venous blood was compared between the experimental group and the control group
IL-1β level in peripheral venous blood
The incidence of IL-1β level (pg/ml) in peripheral venous blood was compared between the experimental group and the control group
cortisol level in peripheral venous blood
The incidence of cortisol level (μg/dL) in peripheral venous blood was compared between the experimental group and the control group

Full Information

First Posted
June 20, 2022
Last Updated
September 29, 2022
Sponsor
Xuzhou Central Hospital
Collaborators
The Affiliated Hospital of Xuzhou Medical University, The First People's Hospital of Xuzhou
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1. Study Identification

Unique Protocol Identification Number
NCT05439707
Brief Title
Effects of Perioperative Transauricular Vagus Nerve Electrical Stimulation on POD, POCD and CPSP
Official Title
Effects of Perioperative Transauricular Vagus Nerve Electrical Stimulation on Postoperative Delirium, Postoperative Cognitive Dysfunction and Chronic Postsurgical Pain in Patients Undergoing Arthroplasty.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 1, 2022 (Anticipated)
Primary Completion Date
July 1, 2024 (Anticipated)
Study Completion Date
September 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Xuzhou Central Hospital
Collaborators
The Affiliated Hospital of Xuzhou Medical University, The First People's Hospital of Xuzhou

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
Yes

5. Study Description

Brief Summary
Postoperative delirium (POD) and postoperative cognitive dysfunction (POCD) occur in 11-51% of patients after surgery, and its prevalence increases with age. The occurrence of delirium is associated with increased morbidity and mortality, prolonged hospital stay, worse functional recovery. Orthopedic procedures and specifically joint replacements have been considered as a major risk for development of chronic postsurgical pain (CPSP). Approximately 13-44% of patients will develop CPSP after knee or hip arthOpioid abuseroplasty. CPSP may cause the discomfort, distress, disability and opioid abuse. Mounting evidence has revealed that inflammation triggered by surgical trauma plays a key role in POD, POCD and CPSP. Recent studies found that vagus nerve stimulation showed the suppression of inflammation. In this study, the effect of perioperative transauricular vagus nerve stimulation on the prognosis of patients undergoing arthroplasty will be investigated, providing potential solutions for the prevention and treatment of postoperative cognitive dysfunction, postoperative delirium and chronic postsurgical pain.
Detailed Description
The investigators assessed POD by the Confusion Assessment Method for the ICU twice daily for 7 days after surgery. Participants' cognitive function was assessed with neuropsychological battery tests. The tests included digit span (forward and backward), Corsi block, paired associate verbal learning, digit symbol test, trail-making test and so on.The investigators make a CPSP diagnosis based on the 11th revision of the International Classification of Diseases.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Cognitive Dysfunction, Postoperative Delirium, Chronic Post Operative Pain

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental group
Arm Type
Experimental
Arm Description
The transaricular vagus nerve stimulator was placed in the left ear trunk, which is dominated only by the auricular branch of the vagus nerve. Continuous stimulation was performed at a frequency of 25Hz with pulse width of 300 μs. The stimulation was adjusted to be higher than the perception threshold and lower than the pain threshold. Each stimulation lasted for 30 minutes, three times per day (morning, noon, evening), from 1 day before surgery to 7 days after surgery, and the treatment lasted for 9 consecutive days.
Arm Title
Control group
Arm Type
Sham Comparator
Arm Description
The transaricular vagus nerve stimulator was placed in the same position as the experimental group, covered with an insulating film and placed at the site of the stimulation, so that the patient could not actually receive the electrical stimulation. Continuous stimulation was performed at a frequency of 25Hz and pulse width of 300 μs, and the stimulation was adjusted to be higher than the perception threshold and lower than the pain threshold. Each stimulation lasted for 30 minutes, three times per day (morning, noon, evening), from 1 day before surgery to 7 days after surgery, for 9 consecutive days.
Intervention Type
Device
Intervention Name(s)
transaricular vagus nerve stimulation
Intervention Description
The transaricular vagus nerve stimulator was placed in the left ear trunk, which is dominated only by the auricular branch of the vagus nerve. Continuous stimulation was performed at a frequency of 25Hz with pulse width of 300 μs. The stimulation was adjusted to be higher than the perception threshold and lower than the pain threshold. Each stimulation lasted for 30 minutes, three times per day (morning, noon, evening), from 1 day before surgery to 7 days after surgery, and the treatment lasted for 9 consecutive days.
Intervention Type
Device
Intervention Name(s)
fake transaricular vagus nerve stimulation
Intervention Description
The transaricular vagus nerve stimulator was placed in the same position as the experimental group, covered with an insulating film and placed at the site of the stimulation, so that the patient could not actually receive the electrical stimulation. Continuous stimulation was performed at a frequency of 25Hz and pulse width of 300 μs, and the stimulation was adjusted to be higher than the perception threshold and lower than the pain threshold. Each stimulation lasted for 30 minutes, three times per day (morning, noon, evening), from 1 day before surgery to 7 days after surgery, for 9 consecutive days.
Primary Outcome Measure Information:
Title
Postoperative cognitive function
Description
The incidence of POCD was compared between the experimental group and the control group.The preoperative and postoperative differences of the following scales were calculated and compared: Digit Span (forward and backward), Visual Retention and Paired Associate Verbal Learning subtests of the Wechsler Memory Scale, Digit Symbol subtest of the Wechsler Adult Intelligence ScaleRevised, Halstead-Reitan Trail Making Test (Part A), Corsi Block Test and Grooved Pegboard Test (favored and unfavored hand). The standard deviation (SD) for each test was computed from the preoperative scores. A participant whose postoperative performance declined by ≥1 SD as compared to each preoperative test score on ≥2 tests was classified as POCD.
Time Frame
1 month after the surgery.
Title
Postoperative cognitive function
Description
The incidence of POCD was compared between the experimental group and the control group.The preoperative and postoperative differences of the following scales were calculated and compared: Digit Span (forward and backward), Visual Retention and Paired Associate Verbal Learning subtests of the Wechsler Memory Scale, Digit Symbol subtest of the Wechsler Adult Intelligence ScaleRevised, Halstead-Reitan Trail Making Test (Part A), Corsi Block Test and Grooved Pegboard Test (favored and unfavored hand). The standard deviation (SD) for each test was computed from the preoperative scores. A participant whose postoperative performance declined by ≥1 SD as compared to each preoperative test score on ≥2 tests was classified as POCD.
Time Frame
3 months after the surgery.
Title
Postoperative delirium
Description
The incidence of POD was compared between the experimental group and the control group.Postoperative delirium was assessed by the Delirium Assessment Scale (CAM-ICU)
Time Frame
Consecutive 7 days after the surgery
Title
Acute postoperative pain
Description
The incidence of acute postoperative pain was compared between the experimental group and the control group.Acute postoperative pain was assessed by Visual Analogue Scale(VAS) for 7 consecutive days within 1 week after surgery.
Time Frame
Consecutive 7 days after the surgery for acute pain
Title
Chronic Postsurgical pain
Description
The incidence of chronic postoperative pain (CPSP) was assessed by the Short Form McGill Pain Questionnaire (SF-MPQ) and Neuropathic Pain Scale (NPS).The incidence of CPSP was compared between the experimental group and the control group.
Time Frame
3 months after the surgery for chronic pain
Secondary Outcome Measure Information:
Title
TNF-α level in peripheral venous blood
Description
The incidence of TNF-α level (pg/ml) in peripheral venous blood was compared between the experimental group and the control group
Time Frame
1 day before the surgery, Postoperative day 1, 3, 5
Title
IL-6 level in peripheral venous blood
Description
The incidence of IL-6 level (pg/ml) in peripheral venous blood was compared between the experimental group and the control group
Time Frame
1 day before the surgery, Postoperative day 1, 3, 5
Title
IL-1β level in peripheral venous blood
Description
The incidence of IL-1β level (pg/ml) in peripheral venous blood was compared between the experimental group and the control group
Time Frame
1 day before the surgery, Postoperative day 1, 3, 5
Title
cortisol level in peripheral venous blood
Description
The incidence of cortisol level (μg/dL) in peripheral venous blood was compared between the experimental group and the control group
Time Frame
1 day before the surgery, Postoperative day 1, 3, 5

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 50 to 80 years old. ASA grade I-Ⅲ. elective knee or hip replacement. Exclusion Criteria: Mini-Mental State Examination (MMSE) score < 23. Education years<7. Peptic ulcer disease, serious cardiac-cerebral vascular disease. Neurological or psychiatric disorders. History of drug and alcohol abuse. Hepatic and/or kidney dysfunction. BMI>35. Patients on antidepressants. ASA >Ⅲ.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yangzi Zhu, Doctor
Phone
+86 18168779150
Email
zhuyz@188.com
First Name & Middle Initial & Last Name or Official Title & Degree
Rui Yao, Maser
Phone
+86 18761341804
Email
yaorui_edu@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yangzi Zhu, Doctor
Organizational Affiliation
Xuzhou Central Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Liwei Wang, Doctor
Organizational Affiliation
Xuzhou Central Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Junli Cao, PhD & MD
Organizational Affiliation
Xuzhou Medical University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Daqing Ma, PhD & MD
Organizational Affiliation
Imperial College London
Official's Role
Study Chair
Facility Information:
Facility Name
Xuzhou Central Hospital
City
Changzhou
State/Province
Jiangsu
ZIP/Postal Code
221009
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xianchi Li, PhD
Phone
+86-0516-83956044
Email
xzzxyykjk@163.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30983589
Citation
Glare P, Aubrey KR, Myles PS. Transition from acute to chronic pain after surgery. Lancet. 2019 Apr 13;393(10180):1537-1546. doi: 10.1016/S0140-6736(19)30352-6.
Results Reference
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PubMed Identifier
28134653
Citation
Lavand'homme P. Transition from acute to chronic pain after surgery. Pain. 2017 Apr;158 Suppl 1:S50-S54. doi: 10.1097/j.pain.0000000000000809. No abstract available.
Results Reference
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PubMed Identifier
24517920
Citation
Hovens IB, Schoemaker RG, van der Zee EA, Absalom AR, Heineman E, van Leeuwen BL. Postoperative cognitive dysfunction: Involvement of neuroinflammation and neuronal functioning. Brain Behav Immun. 2014 May;38:202-10. doi: 10.1016/j.bbi.2014.02.002. Epub 2014 Feb 8.
Results Reference
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PubMed Identifier
31834869
Citation
Eckenhoff RG, Maze M, Xie Z, Culley DJ, Goodlin SJ, Zuo Z, Wei H, Whittington RA, Terrando N, Orser BA, Eckenhoff MF. Perioperative Neurocognitive Disorder: State of the Preclinical Science. Anesthesiology. 2020 Jan;132(1):55-68. doi: 10.1097/ALN.0000000000002956.
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Citation
Jin Z, Hu J, Ma D. Postoperative delirium: perioperative assessment, risk reduction, and management. Br J Anaesth. 2020 Oct;125(4):492-504. doi: 10.1016/j.bja.2020.06.063. Epub 2020 Aug 11.
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Mohanty R, Lindroth H, Twadell S, Nair VA, Prabhakaran V, Sanders RD. A pilot study of neural correlates of perioperative executive function associated with noncardiac surgery in the elderly. Br J Anaesth. 2019 Nov;123(5):e517-e518. doi: 10.1016/j.bja.2019.08.001. Epub 2019 Aug 30. No abstract available.
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Effects of Perioperative Transauricular Vagus Nerve Electrical Stimulation on POD, POCD and CPSP

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