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Effect of transcutaneous electrical acupoint stimulation on blood pressure variability in patients with acute ischemic stroke undergoing intravenous thrombolysis

A clinical randomized controlled study of transcutaneous electrical acupoint stimulation for blood pressure variability in intravenous thrombolysis for stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN64341199
Enrollment
132
Registered
2025-06-28
Start date
2025-03-30
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ultra-early blood pressure variability in patients with acute ischemic stroke treated with intravenous thrombolysis Circulatory System

Interventions

Participants will be randomly allocated (1:1) to either the treatment or the control group. One group will receive transcutaneous electrical acupoint stimulation for approximately 1 hour, from the beg

Sponsors

Beijing Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. No gender limit 2. Age =18 years old 3. Meet the diagnostic criteria of acute ischemic stroke 4. Consistent with the indications of intravenous thrombolysis

Exclusion criteria

Exclusion criteria: 1. Coagulopathy, severe liver and kidney dysfunction 2. Implantation of metal or electronic implantable devices such as a cardiac pacemaker 3. History of epilepsy 4. Being pregnant or breastfeeding, or intending to become pregnant within the next 6 months 5. Damage, inflammation, scar, etc. on the skin of the acupoints; Sensory disturbance or allergy to electrical stimulation) 6. Patients could not tolerate transcutaneous electrical stimulation

Design outcomes

Primary

MeasureTime frame
1. Blood pressure values measured using a mercury sphygmomanometer at baseline, 15, 30, 45, and 60 min after the start of thrombolysis, and 10 min after the completion of thrombolysis 2. Calculated blood pressure variability values measured using data collected during the above 7 blood pressure values monitoring at baseline, 15, 30, 45, and 60 min after the start of thrombolysis, and 10 min after the completion of thrombolysis

Secondary

MeasureTime frame
1. The level of alertness and agitated behavior in patients measured using the Richmond Agitation-Sedation Scale (RASS) at baseline, 30 and 60 min 2. The severity of a stroke measured using the National Institutes of Health Stroke Scale (NIHSS) at baseline, 30 and 60 min 3. The occurrence of adverse events (during thrombolysis: fluctuation of symptoms, aggravation of disease, forced cessation of thrombolysis, various bleeding, application of antihypertensive drugs, application of sedative drugs; after thrombolysis: ischemia aggravation, cerebral hemorrhage, rescue use of antihypertensive drugs, etc.) measured using data observed and recorded during the process of intravenous thrombolysis at any time

Countries

China

Contacts

Public ContactJiaxuan Chen
cjx20252025@163.com+86 (0)13269211249

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026