The Efficacy and Safety of Acupuncture for Prophylaxis of Menstrually Related Migraine

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorGuang'anmen Hospital of China Academy of Chinese Medical Sciences

About this trial

Acupuncture is commonly used for the prevention of migraine and tension-type headaches, and has been found to be effective in reducing both the frequency and severity of these conditions. However, studies on acupuncture for menstrually related migraine (MRM) are limited, and current research has not been able to determine whether its efficacy is due to the actual therapeutic effects of acupuncture or psychological benefits. To address this issue, the investigators have designed a clinical trial to evaluate the efficacy of acupuncture for MRM.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

meet the diagnostic criteria for MRM according to the ICHD-3, with a documented history of MRM for at least 12 months;

have a confirmed diagnosis of migraine by a neurologist;

aged 18-45 years;

have regular menstrual cycles (28 ± 7 days) with menstruation lasting 3-7 days;

Disqualifiers

irregular menstrual cycles, defined as cycle length outside the range of 28±7 days or menstruation duration <3 days or >7 days;

presence of secondary headache disorders, facial neuralgia, or cranial neuralgia;

combined with serious primary diseases such as cardiovascular, hepatic, renal, gastrointestinal, or hematological disorders that may interfere with the treatment protocol, or comorbid neurological conditions such as epilepsy, parkinson's disease, or other central nervous system disorders;

headache symptoms caused by other conditions, such as moderate to severe head or neck trauma, perimenstrual infections, intracranial tumors, intracranial infections, endocrine or metabolic disorders;

Trial design

Design model

Parallel

Treatments tested in this trial

  • electroacupuncture

    Device

    The supine position, the local skin of the acupoints was routinely sterilized, and the selected acupoints were pasted with Acupuncture auxiliary device. The main acupuncture points are DU20, bilateral EX-HN5, ST8, GB20, GB20, LI4, LR3, ST40. Select compatible acupoints based on the patient's accompanying symptoms: 1.Discomfort in the neck: EX-B2 of Cervical 3-4; 2.Emotional anxiety, depression or sleep disorders: GV29, HT7; 3.Stomach or abdominal discomfort: CV12, ST25 and CV6. The disposable acupuncture needles and the electronic acupuncture treatment instrument SDZ-V nerve and muscle intimulator both manufactured by Suzhou Medical Appliance Factory Co., Ltd., China.The specifications of acupuncture needles are Φ0.30×25mm, Φ0.30×40mm. The needles will be inserted into the skin of acupuncture points and manipulated manually by using the techniques such as lifting, thrusting, and twirling, until the internal compound sensation known as deqi.

  • Sham electroacupuncture

    Device

    The SEA group will use Hua Tuo brand disposable blunt-tip sham needles (Φ0.3mm×25mm) and the electronic acupuncture treatment instrument SDZ-V nerve and muscle intimulator both manufactured by Suzhou Medical Appliance Factory Co., Ltd., China. Sham points 1-2, 3-4, 5-6, and 7-8 are bilaterally located at the midpoints between the following pairs of acupoints: SP19 and EX-UE12, SP6 and LR5, EX-UE1 and HT1, and HT7 and SI8. sham LI4: Bilateral of midpoint between acupoint LI4 and LU9; sham LR3: Bilateral of midpoint between acupoint LR3 and ST44; sham ST40: Bilateral of midpoint between acupoint ST40 and GB35. Compatible acupoints: EX-B2 of Cervical 3-4 horizontal side by 0.5 cun; sham GV29: midpoint between acupoint GV29 and BL2. sham CV12: midpoint between acupoint CV12 and ST21; sham ST25: Bilateral of midpoint between acupoint ST25 and SP15; sham CV6: 3 cun lateral to the level of the CV6; The width of the interphalangeal joint of the patient's thumb was 1 "cun".

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: elecrtoacupuncture group (EA group)Experimental treatment 1 intervention
Group B: Sham elecrtoacupuncture group (sham EA group)Sham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in standardized monthly headache days (SMHD) compared with baseline.

The primary outcome is the change in standardized monthly headache days (SMHD). SMHD are calculated by adjusting the actual number of headache days to a standard 28-day menstrual cycle using the following formula: SMHD = (actual headache days × 28) ÷ individual menstrual cycle length

Time frame
At Week 12 post-treatment

Secondary outcomes

1

change in standardized monthly headache days (SMHD) compared with baseline

Time frame
At Weeks 4 and 8 post-treatment, and at Weeks 16, 20, and 24 during follow-up
2

The proportion of patients with cured MRM

Patients are defined as cured if they no longer met the diagnostic criteria for MRM.

Time frame
At Week 12 post-treatment, and at weeks 16, 20, and 24 during follow-up
3

The responder rate

The responder rate is defined as a minimum of 50 % reduction in SMHD compared with baseline.

Time frame
At Weeks 4, 8, and 12 post-treatment, and at Weeks 16, 20, and 24 during follow-up
4

Change in standardized monthly headache severity score from baseline

Standardized monthly headache severity score = (Actual monthly severity score × 28) ÷ Individual menstrual cycle length.

Time frame
At Weeks 4, 8, and 12 post-treatment, and at Weeks 16, 20, and 24 during follow-up

Other outcomes

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