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Efficacy of Electroacupuncture in NMOSD Patients With Pain: Study Protocol

Primary Purpose

Neuromyelitis Optica Spectrum Disorders, Pain

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
electroacupuncture
Sponsored by
Yuanqi Zhao,MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neuromyelitis Optica Spectrum Disorders

Eligibility Criteria

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

Inclusion Criteria: people diagnosed as NMOSD according to the International Panel for NMO Diagnosis (IPND) criteria.[21] NRS≥4. people were treated with stable doses of biological therapy and/or prednisone, with no regimen adjustment within 30 days prior to enrollment. people did not adjust any standard pain medication combinations, including antiepileptic drugs, antidepressants, and opioids, within 30 days before enrollment. people or their families provided written informed consent. Exclusion Criteria: people enrolled in other clinical studies. people with low cognitive or mental ability. people who became pregnant during the study period, breastfed, or planned to become pregnant. people with serious diseases related to the heart, liver, kidney or hematopoietic system. people with diabetic peripheral neuropathy.

Sites / Locations

  • Guangdong Provincial Hospital of Chinese Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

the electroacupuncture group

the sham electroacupuncture group

Arm Description

electroacupuncture were inserted into bilateral Zusanli (ST36), Sanyinjiao (SP6), Hegu (LI4) and Quchi (LI11), and Yintang (EX-HN3). Electroacupuncture parameters selected the sparse wave, the frequency was 4 Hz, the stimulation intensity was tolerated by the patient.

According to the previous trial,[19] sham acupoints were 1cm away from the level of the acupoints used in the EA group, which avoided the area corresponding to any of the 14 meridians of TCM. The insertion of the needle was shallower (less than 0.2cm) and had similar pain to that of normal needle insertion. The stimulation intensity was 0mA. However, the model of electroacupuncture, the frequency, and duration of treatment in the SEA group were identical in the TA group.

Outcomes

Primary Outcome Measures

Short-Form of McGill Pain Questionnaire(SF - MPQ)
higher scores mean a worse outcome.
Short-Form of McGill Pain Questionnaire(SF - MPQ)
higher scores mean a worse outcome.

Secondary Outcome Measures

Expanded Disability Status Scale(EDSS)
higher scores mean a worse outcome.
Expanded Disability Status Scale(EDSS)
higher scores mean a worse outcome.
numerical rating scale(NRS)
higher scores mean a worse outcome.
numerical rating scale(NRS)
higher scores mean a worse outcome.
Self-Rating Anxiety Scale (SAS)
higher scores mean a worse outcome.
Self-Rating Anxiety Scale (SAS)
higher scores mean a worse outcome.
Self-rating Depression Scale (SDS)
higher scores mean a worse outcome.
Self-rating Depression Scale (SDS)
higher scores mean a worse outcome.
36-item Short-Form (SF-36)
higher scores mean a better outcome.
36-item Short-Form (SF-36)
higher scores mean a better outcome.
Interleukin-6 (IL-6)
higher scores mean a worse outcome.
Interleukin-6 (IL-6)
higher scores mean a worse outcome.
tumor necrosis factor-α (TNF-α)
higher scores mean a worse outcome.
tumor necrosis factor-α (TNF-α)
higher scores mean a worse outcome.

Full Information

First Posted
April 20, 2023
Last Updated
May 20, 2023
Sponsor
Yuanqi Zhao,MD
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1. Study Identification

Unique Protocol Identification Number
NCT05871658
Brief Title
Efficacy of Electroacupuncture in NMOSD Patients With Pain: Study Protocol
Official Title
Efficacy of Electroacupuncture in NMOSD Patients With Pain: Study Protocol
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
March 21, 2022 (Actual)
Primary Completion Date
February 21, 2023 (Actual)
Study Completion Date
February 21, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Yuanqi Zhao,MD

4. Oversight

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

5. Study Description

Brief Summary
Abstract Background Neuropathic pain is a common complication in neuromyelitis optica spectrum disorder (NMOSD), which seriously affects the quality of life of NMOSD patients, with no satisfactory treatment. Through the previous literature study and clinical observation, we found that acupuncture has good curative effect in the treatment of pain, especially electric acupuncture, but thestudies on acupuncture intervention in pain of NMOSD are still scare. Objective To evaluate the clinical efficacy of electroacupuncture on NMOSD patients with pain. Materials and Methods In this exploratory randomized controlled study, NMOSD patients with pain were recruited from March 21, 2022 to February 21, 2023. Patients meeting the inclusion and exclusion criteria were randomly assigned to the electroacupuncture group (experimental group) and the sham electroacupuncture group (control group) by simple random method (envelope method) according to the inclusion order. Totally, there are 20 patients enrolled. The experimental group received electroacupuncture therapy and the control group received sham electroacupuncture therapy. A total of 8 sessions were given twice a week for 30 minutes each. On the baseline, demographic information, medication history, specimens of routine blood, blood biochemistry, liver function, IL - 6, TNF-α were collected, the brain, cervical and thoracic MRI were perfected and collected, patients filled in the SF - MPQ, NRS, SF - 36, SAS, SDS, EDSS. After the treatment, specimens of routine blood, blood biochemistry, liver function, IL - 6, TNF-α were collected again, patients filled in the SF - MPQ, NRS, SF - 36, SAS, SD, EDSS. The main outcome indicators were SF-MPQ, and the secondary outcome indicators were EDSS, NRS, SAS, SDS, SF-36, IL-6, and TNF-α. Conclusion This is the first exploratory randomized controlled study to evaluate the efficacy of electroacupuncture on pain in patients with NMOSD. The study will provide clincial evidence of the practice of electroacupuncture on NMOSD with pain. Key Words neuromyelitis optica spectrum disorders; pain; electroacupuncture

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neuromyelitis Optica Spectrum Disorders, Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
the electroacupuncture group (experimental group) and the sham electroacupuncture group (control group)
Masking
Participant
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
the electroacupuncture group
Arm Type
Experimental
Arm Description
electroacupuncture were inserted into bilateral Zusanli (ST36), Sanyinjiao (SP6), Hegu (LI4) and Quchi (LI11), and Yintang (EX-HN3). Electroacupuncture parameters selected the sparse wave, the frequency was 4 Hz, the stimulation intensity was tolerated by the patient.
Arm Title
the sham electroacupuncture group
Arm Type
Sham Comparator
Arm Description
According to the previous trial,[19] sham acupoints were 1cm away from the level of the acupoints used in the EA group, which avoided the area corresponding to any of the 14 meridians of TCM. The insertion of the needle was shallower (less than 0.2cm) and had similar pain to that of normal needle insertion. The stimulation intensity was 0mA. However, the model of electroacupuncture, the frequency, and duration of treatment in the SEA group were identical in the TA group.
Intervention Type
Behavioral
Intervention Name(s)
electroacupuncture
Intervention Description
electroacupuncture were inserted into bilateral Zusanli (ST36), Sanyinjiao (SP6), Hegu (LI4) and Quchi (LI11), and Yintang (EX-HN3). Electroacupuncture parameters selected the sparse wave, the frequency was 4 Hz, the stimulation intensity was tolerated by the patient.
Primary Outcome Measure Information:
Title
Short-Form of McGill Pain Questionnaire(SF - MPQ)
Description
higher scores mean a worse outcome.
Time Frame
on the baseline
Title
Short-Form of McGill Pain Questionnaire(SF - MPQ)
Description
higher scores mean a worse outcome.
Time Frame
through study completion, an average of 1 month
Secondary Outcome Measure Information:
Title
Expanded Disability Status Scale(EDSS)
Description
higher scores mean a worse outcome.
Time Frame
on the baseline
Title
Expanded Disability Status Scale(EDSS)
Description
higher scores mean a worse outcome.
Time Frame
through study completion, an average of 1 month
Title
numerical rating scale(NRS)
Description
higher scores mean a worse outcome.
Time Frame
on the baseline
Title
numerical rating scale(NRS)
Description
higher scores mean a worse outcome.
Time Frame
through study completion, an average of 1 month
Title
Self-Rating Anxiety Scale (SAS)
Description
higher scores mean a worse outcome.
Time Frame
on the baseline
Title
Self-Rating Anxiety Scale (SAS)
Description
higher scores mean a worse outcome.
Time Frame
through study completion, an average of 1 month
Title
Self-rating Depression Scale (SDS)
Description
higher scores mean a worse outcome.
Time Frame
on the baseline
Title
Self-rating Depression Scale (SDS)
Description
higher scores mean a worse outcome.
Time Frame
through study completion, an average of 1 month
Title
36-item Short-Form (SF-36)
Description
higher scores mean a better outcome.
Time Frame
on the baseline
Title
36-item Short-Form (SF-36)
Description
higher scores mean a better outcome.
Time Frame
through study completion, an average of 1 month
Title
Interleukin-6 (IL-6)
Description
higher scores mean a worse outcome.
Time Frame
on the baseline
Title
Interleukin-6 (IL-6)
Description
higher scores mean a worse outcome.
Time Frame
through study completion, an average of 1 month
Title
tumor necrosis factor-α (TNF-α)
Description
higher scores mean a worse outcome.
Time Frame
on the baseline
Title
tumor necrosis factor-α (TNF-α)
Description
higher scores mean a worse outcome.
Time Frame
through study completion, an average of 1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: people diagnosed as NMOSD according to the International Panel for NMO Diagnosis (IPND) criteria.[21] NRS≥4. people were treated with stable doses of biological therapy and/or prednisone, with no regimen adjustment within 30 days prior to enrollment. people did not adjust any standard pain medication combinations, including antiepileptic drugs, antidepressants, and opioids, within 30 days before enrollment. people or their families provided written informed consent. Exclusion Criteria: people enrolled in other clinical studies. people with low cognitive or mental ability. people who became pregnant during the study period, breastfed, or planned to become pregnant. people with serious diseases related to the heart, liver, kidney or hematopoietic system. people with diabetic peripheral neuropathy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhao yuan qi, Dr
Organizational Affiliation
Guangdong Provincial Hospital of Traditional Chinese Medicine
Official's Role
Study Director
Facility Information:
Facility Name
Guangdong Provincial Hospital of Chinese Medicine
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510000
Country
China

12. IPD Sharing Statement

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Efficacy of Electroacupuncture in NMOSD Patients With Pain: Study Protocol

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