ClinicalTrials.gg
RecruitingNCT05561088HEALTHUpdated May 12, 2023

Efficacy and Safety of Head Acupuncture After Mechanical Thrombectomy for Acute Ischemic Stroke

An interventional study of Scalp Acupuncture and The treatment recommended in the guidelines for acute ischemic stroke was administered in Acupuncture, Acute Ischemic Stroke and Mechanical Thrombectomy, sponsored by Xi'an No.3 Hospital. Recruiting at 1 site in China. Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2023-05-12.

Sponsored by Xi'an No.3 Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Feb 2026, 8 months ago, but the record still lists the study as recruiting.
  • Started Apr 2023; still recruiting 3 years 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
272
Allocation
Randomized
Ages
18 Years to 100 Years
Sex
All
01

Study summary

To evaluate the efficacy and safety of head acupuncture combined with endovascular therapy for cerebral infarction compared with endovascular therapy alone

Read the detailed description

Control group: Mechanical thrombectomy followed by the guideline recommended treatment for acute ischemic stroke;

Experimental group: After mechanical thrombectomy, head acupuncture and the treatment regimen recommended by the guideline for acute ischemic stroke were administered

02

Conditions studied

  • Acupuncture
  • Acute Ischemic Stroke
  • Mechanical Thrombectomy

Browse trials for

03

In context

Ischemic Stroke

2,612 studies on the registry are indexed under Ischemic Stroke; 971 are open to participants now.

This study's planned enrollment of 272 is above the median of 120 across 1,776 interventional studies indexed under Ischemic Stroke.

Browse Ischemic Stroke studies →

Lead sponsor

Xi'an No.3 Hospital is the lead sponsor of 7 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age ≥18 years;
  • Patients with acute ischemic stroke who received endovascular treatment within 24 hours of onset;
  • 6 \< NIHSS ≤25;
  • ASPECT score ≥6 points;
  • Signed .

Exclusion criteria

Exclusion Criteria:

  • CT or brain MRI confirmed intracranial tumor and intracranial hemorrhage;
  • of contrast media;
  • Dementia or mental illness,unable to cooperate with treatment and follow-up;
  • The expected survival time was less than 3 months;
  • Women who are pregnant, planning to become pregnant or breastfeeding;
  • Currently participating in other clinical trials.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
272 participants (estimated)

Study arms

  • Experimental
    experimental group

    Mechanical thrombectomy was followed by acupuncture and guideline-based conventional treatment

    Other: Scalp Acupuncture · Other: The treatment recommended in the guidelines for acute ischemic stroke was administered

  • Experimental
    control group

    Conventional treatment based on guidelines was administered after mechanical thrombectomy

    Other: The treatment recommended in the guidelines for acute ischemic stroke was administered

Interventions

  • OtherScalp Acupuncture

    mplementation plan of head needle: The middle frontal line (MS1), the middle parietal line (MS5) and the back parietal and temporal oblique line (MS7) in the International Standardization Program for the Name of the first needle Point in 1989 were selected, and the needles were inserted along the shape of each section. One needle was inserted into the middle frontal line and the middle parietal line, and two needles were inserted into the back parietal and temporal oblique line. The KWD-808I pulse electrotherapy instrument produced by Changzhou Wujin Great Wall Medical Equipment Co., Ltd. is used on the needle handle after lifting, inserting and twisting. The continuous waveform was used, the voltage was 2-4 V, the frequency was 60-80 times /min, the intensity was tolerated by the patient, the needle was kept for 30min, and the treatment was performed once a day.

  • OtherThe treatment recommended in the guidelines for acute ischemic stroke was administered

    The treatment recommended in the guidelines for acute ischemic stroke was administered

06

What researchers measure

Primary outcomes

  1. Ratio of Modified rankin scale (mRS) score ≤2

    The modified rankin Scale (mRS) score ≤2 indicates that the patient has the ability to live independently.

    Time frame: 90 days after onset

Secondary outcomes

  1. National Institute of Health stroke scale(NIHSS) score

    NIHSS scores range from 0 to 42, with higher scores indicating more severe nerve damage.

    Time frame: 10 days after onset

  2. Modified rankin scale (mRS) score

    Modified rankin scale (mRS) Score is used to measure the neurological function recovery status of patients after stroke, and its score ranges from 0 to 6

    Time frame: 90 days after onset

  3. Incidence of cerebral hemorrhage

    No hemorrhage was found on the first head CT/MRI after cerebral infarction, but intracranial hemorrhage was found on the second head CT/MRI

    Time frame: 7 days after randomization

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 12, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05561088
Lead sponsor
Xi'an No.3 Hospital
Responsible party
Sponsor
First posted
Sep 30, 2022
Start date
Apr 27, 2023
Primary completion
Feb 28, 2026 (estimated)
Completion
Oct 31, 2028 (estimated)
Last update
May 12, 2023

Study contacts

Shilin L i, Doctor
Contact
lihuashiling@126.com
8615398076154
Mingze Chang, Doctor
Contact
cbangingze191@163.com
8615609250898

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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