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A Randomized Controlled Trial of Acupuncture in Treating Migraine

Primary Purpose

Migraine Without Aura

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Acupuncture combined with placebo
Sham acupuncture combined with flunarizine hydrochloride
Sponsored by
The Third Affiliated hospital of Zhejiang Chinese Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Migraine Without Aura focused on measuring migraine, acupuncture, randomized controlled trial

Eligibility Criteria

25 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients meet the diagnostic criteria of migraine without aura;
  2. 25 ≤ age ≤50 years, male or female;
  3. The efficacy of drugs and other therapeutic methods is not obvious; the frequency of migraine attacks in the past 3 months is more than twice a month;
  4. Drug treatment for migraine without aura is stopped for at least one week;
  5. Participants can understand the study protocol and written informed consent is signed.

Exclusion Criteria:

  1. Patients have severe complications in cardiovascular, liver, kidney, hematopoietic and other systems;
  2. Pregnant or lactating women;
  3. Patients have spontaneous bleeding tendency so it is not suitable for them to receive acupuncture;
  4. Patients have an allergic history of flunarizine hydrochloride or a history of depression;
  5. Patients are diagnosed as psychosis.

Sites / Locations

  • The Third Affiliated Hospital of Zhejiang Chinese Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Acupuncture combined with placebo group

Sham acupuncture combined with medication group

Arm Description

Patients in this group will receive acupuncture combined with placebo.

Participants in this group will receive sham acupuncture plus flunarizine hydrochloride.

Outcomes

Primary Outcome Measures

Change in pain intensity
Change in Pain intensity will be measured by visual analog scale (VAS),he VAS divides the pain from 0 to 10 into 11 grades. 0: No pain; 10: the worst pain; ≤3: mild pain; 4-6: moderate pain which is tolerable; 7-10: severe pain which is unbearable.
Change in number of migraine attacks per 4 weeks
Change in Number of migraine attacks is assessed by patients' pain diary

Secondary Outcome Measures

Migraine-specific Quality of life
Quality of life will be measure by migraine-specific quality of life (MSQOL) scale.This questionnaire consists of 25 items, with 4 answers for each question. The overall format and scores are as follows: 1.Very much; 2. Many; 3. Some; 4. Not at all. The overall scale ranges from 25 to 100, with higher scores indicating the better quality of life.
Headache Needs Assessment Survey (HANA) Questionnaire Scale
Evaluate the frequency and severity of the migraine effect.The overall score ranges from 14 to 70, with higher scores indicating the greater impact of migraine on life.

Full Information

First Posted
February 17, 2021
Last Updated
July 8, 2022
Sponsor
The Third Affiliated hospital of Zhejiang Chinese Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT04766762
Brief Title
A Randomized Controlled Trial of Acupuncture in Treating Migraine
Official Title
A Randomized Controlled Trial of Acupuncture in Treating Migraine Without Aura by the Method of Regulating Ying and Wei
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 21, 2021 (Actual)
Primary Completion Date
January 1, 2023 (Anticipated)
Study Completion Date
February 28, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Third Affiliated hospital of Zhejiang Chinese Medical University

4. Oversight

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

5. Study Description

Brief Summary
Migraine without aura is a common kind of nervous system diseases that can easily cause recurrent headache, leading to severe impacts on quality of life and health care costs. Current therapeutic options for migraine without aura mainly include flunarizine hydrochloride that can relieve vasospasm. Nevertheless, the efficacy of flunarizine hydrochloride is always limited by inevitable side effects, which result in poor compliance of patients. Moreover, for some most suffering patients, the control of pain is often unsatisfactory despite of the administration of complex treatment combinations. As a non-pharmaceutical therapy, acupuncture is widely used for a wide range of pain conditions. Thus, it might be an alternative treatment for migraine without aura. The aim of this randomized controlled trial is to investigate the efficacy and safety of acupuncture therapy in patients with migraine without aura from the perspective of Regulating Ying and Wei.
Detailed Description
This randomized controlled trial will enroll 96 migraine patients without aura from the Third Affiliated Hospital of Zhejiang Chinese Medical University. All patients will be randomly assigned to either the acupuncture combined with placebo group or sham acupuncture combined with medication group through a randomization system. Primary outcome will be pain intensity assessed by visual analogue scale (VAS) scale. Secondary outcomes will include migraine-specific quality of life (MSQOL) scale and headache needs assessment survey (HANA) questionnaire scale.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine Without Aura
Keywords
migraine, acupuncture, randomized controlled trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
96 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Acupuncture combined with placebo group
Arm Type
Experimental
Arm Description
Patients in this group will receive acupuncture combined with placebo.
Arm Title
Sham acupuncture combined with medication group
Arm Type
Other
Arm Description
Participants in this group will receive sham acupuncture plus flunarizine hydrochloride.
Intervention Type
Procedure
Intervention Name(s)
Acupuncture combined with placebo
Intervention Description
This group will include 48 patients. Patients in this group will receive acupuncture combined with placebo. Participants are in the supine position. The bilateral Tianrong (SI 17) acupoints are needled for 1-1.5 inch with the direction tilted back 45±5 degrees. The bilateral Fengchi (GB 20) acupoints are needled for 0.5-1 inch with the direction tilted to nose. The bilateral Neiguan (PC 6) acupoints are also needled for 0.5-1 inch with the straight direction. In addition, 4-6 additional acupoints can be identified according to different syndrome types of patients. The needles are kept for 30 min, the treatment frequency is 3 times per week, and the treatment duration lasts 8 weeks. Meanwhile, the dosage of placebo is 1 capsule twice a day and the treatment duration also lasts 8 weeks.
Intervention Type
Procedure
Intervention Name(s)
Sham acupuncture combined with flunarizine hydrochloride
Intervention Description
This group will include 48 patients. Participants in this group will receive sham acupuncture plus flunarizine hydrochloride. Participants are in the supine position and sham acupuncture is conducted. The bilateral Tianrong (SI 17) acupoints, Fengchi (GB 20) acupoints and Neiguan (PC 6) acupoints are selected, and 4-6 additional acupoints can be identified according to the syndrome type of the participants. The needles are kept for 30 min, the treatment frequency is 3 times per week, and the treatment duration lasts 8 weeks. Moreover, the dosage of flunarizine hydrochloride is 5mg twice a day and the treatment duration also lasts 8 weeks.
Primary Outcome Measure Information:
Title
Change in pain intensity
Description
Change in Pain intensity will be measured by visual analog scale (VAS),he VAS divides the pain from 0 to 10 into 11 grades. 0: No pain; 10: the worst pain; ≤3: mild pain; 4-6: moderate pain which is tolerable; 7-10: severe pain which is unbearable.
Time Frame
Baseline,4 weeks after treatment,8 weeks after treatment,4 weeks after follow-up visiting,12 weeks after follow-up visiting,and 24 weeks after follow-up visiting
Title
Change in number of migraine attacks per 4 weeks
Description
Change in Number of migraine attacks is assessed by patients' pain diary
Time Frame
Baseline,4 weeks after treatment,8 weeks after treatment,4 weeks after follow-up visiting,12 weeks after follow-up visiting,and 24 weeks after follow-up visiting
Secondary Outcome Measure Information:
Title
Migraine-specific Quality of life
Description
Quality of life will be measure by migraine-specific quality of life (MSQOL) scale.This questionnaire consists of 25 items, with 4 answers for each question. The overall format and scores are as follows: 1.Very much; 2. Many; 3. Some; 4. Not at all. The overall scale ranges from 25 to 100, with higher scores indicating the better quality of life.
Time Frame
Baseline,4 weeks after treatment,8 weeks after treatment,4 weeks after follow-up visiting,12 weeks after follow-up visiting,and 24 weeks after follow-up visiting
Title
Headache Needs Assessment Survey (HANA) Questionnaire Scale
Description
Evaluate the frequency and severity of the migraine effect.The overall score ranges from 14 to 70, with higher scores indicating the greater impact of migraine on life.
Time Frame
Baseline,4 weeks after treatment,8 weeks after treatment,4 weeks after follow-up visiting,12 weeks after follow-up visiting,and 24 weeks after follow-up visiting

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients meet the diagnostic criteria of migraine without aura; 25 ≤ age ≤50 years, male or female; The efficacy of drugs and other therapeutic methods is not obvious; the frequency of migraine attacks in the past 3 months is more than twice a month; Drug treatment for migraine without aura is stopped for at least one week; Participants can understand the study protocol and written informed consent is signed. Exclusion Criteria: Patients have severe complications in cardiovascular, liver, kidney, hematopoietic and other systems; Pregnant or lactating women; Patients have spontaneous bleeding tendency so it is not suitable for them to receive acupuncture; Patients have an allergic history of flunarizine hydrochloride or a history of depression; Patients are diagnosed as psychosis.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chuanlong Zhou
Phone
15868486255
Email
471388079@qq.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chuanlong Zhou
Organizational Affiliation
The Third Affiliated hospital of Zhejiang Chinese Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Third Affiliated Hospital of Zhejiang Chinese Medical University
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chuanlong Zhou, MM
Phone
15868486255
Ext
86
Email
471388079@qq.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35957963
Citation
Zhou C, Bao J, Hu H, Ye S, Shao X, Liang Y, Fang J. Acupuncture Based on Regulating Autonomic Nerves for the Prevention of Migraine Without Aura: A Prospective, Double-Dummy, Randomized Controlled Clinical Trial. J Pain Res. 2022 Aug 4;15:2211-2221. doi: 10.2147/JPR.S372311. eCollection 2022.
Results Reference
derived

Learn more about this trial

A Randomized Controlled Trial of Acupuncture in Treating Migraine

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