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Effect of Electroacupuncture on Sepsis-induced Intestinal Dysfunction

Primary Purpose

Sepsis, Intestinal Dysfunction

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
electroacupuncture treatment
sham electroacupuncture treatment
Sponsored by
Jianbo Yu
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sepsis focused on measuring sepsis, electroacupuncture, intestinal dysfunction

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Meet the diagnostic criteria of sepsis 3.0
  2. AGI grade II or above,
  3. At least 18 years old
  4. Volunteer to participate in this study and sign the informed consent form

Exclusion Criteria:

  1. Patients with bowel dysfunction caused by other diseases or surgical operations
  2. Those who have chronic gastrointestinal diseases such as Crohn's disease and ulcerative colitis
  3. Those who have recently used gastrointestinal motility drugs and within 5 times the half-life
  4. Those who are participating in other drug clinical trials
  5. Refuse to participate in this study

Sites / Locations

  • Electroacupuncture Apparatus

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

electroacupuncture treatment

sham electroacupuncture treatment

Arm Description

Participants in the treatment group underwent 60 minutes acupuncture (0.30mm×70mm) at ST36 (Zusanli) and ST37 (Shangjuxu) twice a day for seven days. After"Deqi",electroacupuncture stimulation apparatus (HANS G6805-2, Huayi Co, Shanghai, China) isconnected and maintained the end of treatment

sham electroacupuncture treatment participants in the control group received shallow needling (0.30mm×25mm) at ST36 and ST37(nonacupoints located 1 inch beside acupoints, about 20mm). Specifically, the depth of needle insertion into nonacupoints is 3-5mm and avoided manual stimulation and no "Deqi" without actual current output.

Outcomes

Primary Outcome Measures

The effect on intestinal motility
Record the serum levels of motilin of the two groups
The effect on intestinal motility
Record the serum levels of gastrin of the two groups
The effect on intestinal barrier
Record serum levels of DAO of the two groups
The effect on intestinal barrier
Record serum levels of I-FABP of the two groups

Secondary Outcome Measures

Duration of mechanical ventilation in patients with endotracheal intubation in ICU
Duration of mechanical ventilation and endotracheal intubation in ICU
Length of stay in hospital
ICU stay time and hospitalization time
All-cause 28-day mortality
All reasons (such as infection, hemorrhage) caused the mortality during the first 28 days

Full Information

First Posted
November 22, 2020
Last Updated
November 25, 2020
Sponsor
Jianbo Yu
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1. Study Identification

Unique Protocol Identification Number
NCT04646629
Brief Title
Effect of Electroacupuncture on Sepsis-induced Intestinal Dysfunction
Official Title
Effect of Electroacupuncture on Sepsis-induced Intestinal Dysfunction: a Prospective, Double-blind, Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 23, 2020 (Anticipated)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
June 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jianbo Yu

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
Title: Effect of electroacupuncture on sepsis-induced intestinal dysfunction Research center: single center The Design of the study: Randomized, double-blind, controlled study The population of the study: The patients over 18 years that met the criteria of sepsis3.0 and with AGI grade II or above are enrolled in the study Sample size: Enroll 60 patients (30patients in each group) Interventions: Participants in the treatment group underwent 60 minutes acupuncture (0.30mm×70mm) at ST36 (Zusanli) and ST37 (Shangjuxu) twice a day for seven days. After"Deqi",electroacupuncture stimulation apparatus (HANS G6805-2, Huayi Co, Shanghai, China) is connected and maintained the end of treatment. Participants in the control group received shallow needling (0.30mm×25mm) at ST36 and ST37(nonacupoints located 1 inch beside acupoints, about 20mm). Specifically, the depth of needle insertion into nonacupoints is 3-5mm and avoided manual stimulation and no "Deqi" without actual current output. The aim of the research: To investigate the effect of electroacupuncture on sepsis-induced intestinal dysfunction. Outcome# 1) Primary outcome: The intestinal function indicators including: 1) Clinical symptoms: bowel sounds, intra-abdominal pressure, time to first exhaust/defecation, daily tolerable enteral nutrition 2) Intestinal motility indicators: the levels of serum motilin and gastrin 3) Intestinal barrier indicators: the levels of serum diamine oxidase (DAO), D-lactic acid and I-FABP 2)Secondary outcome# Duration of mechanical ventilation in patients with endotracheal intubation on ICU admission; Length of stay in ICU and Length of stay in hospital; 30-day life quality and cognitive function after surgery; All-cause 28-day mortality. The estimated duration of the study#1-2years.
Detailed Description
This study is a randomized, double-blinded, placebo controlled and long-term follow-up design. In this study, ST36 (Zusanli) and ST37 (Shangjuxu) were selected for electroacupuncture treatment, accompanied with evaluating the effects on intestinal function in septic patients. Meanwhile, the blood biochemical indexes such as heme oxygenase-1(HO-1), PTEN induced putative kinase 1(PINK1), polo-like kinase 1(PLK1) and interleukin-6 are detected. To clarify the effect of electroacupuncture on sepsis-induced intestinal dysfunction is of great significance to the clinical applications and popularization of traditional acupuncture treatment across the world.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sepsis, Intestinal Dysfunction
Keywords
sepsis, electroacupuncture, intestinal dysfunction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
electroacupuncture treatment
Arm Type
Experimental
Arm Description
Participants in the treatment group underwent 60 minutes acupuncture (0.30mm×70mm) at ST36 (Zusanli) and ST37 (Shangjuxu) twice a day for seven days. After"Deqi",electroacupuncture stimulation apparatus (HANS G6805-2, Huayi Co, Shanghai, China) isconnected and maintained the end of treatment
Arm Title
sham electroacupuncture treatment
Arm Type
Sham Comparator
Arm Description
sham electroacupuncture treatment participants in the control group received shallow needling (0.30mm×25mm) at ST36 and ST37(nonacupoints located 1 inch beside acupoints, about 20mm). Specifically, the depth of needle insertion into nonacupoints is 3-5mm and avoided manual stimulation and no "Deqi" without actual current output.
Intervention Type
Device
Intervention Name(s)
electroacupuncture treatment
Intervention Description
Participants in the treatment group underwent 60 minutes acupuncture (0.30mm×70mm) at ST36 (Zusanli) and ST37 (Shangjuxu) twice a day for seven days.After "Deqi", electroacupuncture stimulation apparatus (HANS G6805-2, Huayi Co, Shanghai, China) is connected with the density wave (2/100 Hz), width 0.25 ms, intensity of 1 ~ 30 mA (gradually increase to the patient's maximum tolerance) and maintained the end of treatment.
Intervention Type
Device
Intervention Name(s)
sham electroacupuncture treatment
Intervention Description
Participants in the sham electroacupuncture group received shallow needling (0.30mm×25mm) at ST36 and ST37(nonacupoints located 1 inch beside acupoints, about20mm). Specifically, the depth of needle insertion into nonacupoints is 3-5mm and avoided manual stimulation and no "Deqi" without actual current output, and retained the needle for the same time as treatment group
Primary Outcome Measure Information:
Title
The effect on intestinal motility
Description
Record the serum levels of motilin of the two groups
Time Frame
an average of one year
Title
The effect on intestinal motility
Description
Record the serum levels of gastrin of the two groups
Time Frame
an average of 1 year
Title
The effect on intestinal barrier
Description
Record serum levels of DAO of the two groups
Time Frame
up to 1 year
Title
The effect on intestinal barrier
Description
Record serum levels of I-FABP of the two groups
Time Frame
up to 12 months
Secondary Outcome Measure Information:
Title
Duration of mechanical ventilation in patients with endotracheal intubation in ICU
Description
Duration of mechanical ventilation and endotracheal intubation in ICU
Time Frame
one year
Title
Length of stay in hospital
Description
ICU stay time and hospitalization time
Time Frame
up to one year
Title
All-cause 28-day mortality
Description
All reasons (such as infection, hemorrhage) caused the mortality during the first 28 days
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meet the diagnostic criteria of sepsis 3.0 AGI grade II or above, At least 18 years old Volunteer to participate in this study and sign the informed consent form Exclusion Criteria: Patients with bowel dysfunction caused by other diseases or surgical operations Those who have chronic gastrointestinal diseases such as Crohn's disease and ulcerative colitis Those who have recently used gastrointestinal motility drugs and within 5 times the half-life Those who are participating in other drug clinical trials Refuse to participate in this study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yingya Cao, MD
Phone
15055324662
Email
caoyingya1990@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jianbo Yu, PhD
Organizational Affiliation
Tianjin Nankai Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Electroacupuncture Apparatus
City
Tianjin
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yingya Cao, MD
Phone
15055324662
Email
caoyingya1990@126.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30046610
Citation
Meng JB, Jiao YN, Zhang G, Xu XJ, Ji CL, Hu MH, Lai ZZ, Zhang M. Electroacupuncture Improves Intestinal Dysfunction in Septic Patients: A Randomised Controlled Trial. Biomed Res Int. 2018 Jun 26;2018:8293594. doi: 10.1155/2018/8293594. eCollection 2018.
Results Reference
background
PubMed Identifier
27299587
Citation
Yoseph BP, Klingensmith NJ, Liang Z, Breed ER, Burd EM, Mittal R, Dominguez JA, Petrie B, Ford ML, Coopersmith CM. Mechanisms of Intestinal Barrier Dysfunction in Sepsis. Shock. 2016 Jul;46(1):52-9. doi: 10.1097/SHK.0000000000000565.
Results Reference
background
PubMed Identifier
30773861
Citation
Li HF, Hu GQ, Liu WW. [Clinical trials of acupuncture of Jiaji (EX-B2) for treatment of gastrointestinal dysfunction in sepsis patients]. Zhen Ci Yan Jiu. 2019 Jan 25;44(1):43-6. doi: 10.13702/j.1000-0607.170579. Chinese.
Results Reference
background
PubMed Identifier
32270631
Citation
Liu H, Zhu J, Ni HB, Hu XX. [Transcutaneous electrical acupoint stimulation for early enteral nutrition tolerance in patients with sepsis of gastrointestinal dysfunction: a multi-center randomized controlled trial]. Zhongguo Zhen Jiu. 2020 Mar 12;40(3):229-33. doi: 10.13703/j.0255-2930.20190426-0003. Chinese.
Results Reference
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Effect of Electroacupuncture on Sepsis-induced Intestinal Dysfunction

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