Skip to content

Observation on the Neurovascular Protective Effect of Zhongfeng Cuntong Moxibustion in Patients with Ischemic Stroke Based on the Anti-Inflammatory Effect of Vascular Endothelial Cells

Observation on Neurovascular Protection of Stroke Promoting Moxibustion in Patients with Ischemic Stroke Based on Anti-inflammatory Effect of Vascular Endothelial Cells

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112745
Enrollment
Unknown
Registered
2025-11-19
Start date
2025-07-02
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Ischemic Stroke

Interventions

Treatment group:1. Acupoint: Shenque (CV8). 2. Equipment: Medicinal cake, moxibustion box, strap, flame gun, smokeless moxa stick (diameter 1.8 cm, length 20 cm), metal tray. 3. Procedure: (1
(2) Place the moxibustion box over the Shenque point and secure it with a strap
(3) Insert the smokeless moxa stick into the fixed holder on the moxibustion box, ensuring the bottom end of the stick is positioned 2–3 cm above the bottom of the box
(4) Light the moxa stick
during the procedure, continuously adjust the distance between the burning end of the stick and the bottom of the box, and closely monitor to prevent falling embers from causing burns or damaging equi
(5) Each treatment session lasts 60 minutes
(6) After treatment, clean the application site, assist the patient in adjusting clothing, and have them rest in a comfortable position for 5–10 minutes
(7) After the patient returns to the ward, organize and inventory all used materials, and maintain a clean environment in the moxibustion room. 4. Treatment regimen: Continuous treatment for 7 days,
Control group:Routine treatment

Sponsors

Wuxi No.2 People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Meeting the above diagnostic criteria of traditional Chinese and Western medicine; 2. Aged 20–80 years, regardless of gender; 3. Disease duration between 2 weeks and 6 months; 4. With neurological impairment, clear consciousness, stable clinical signs, and able to cooperate with all assessments; 5. Provided informed consent and signed the informed consent form personally.

Exclusion criteria

Exclusion criteria: 1. Those who do not meet the diagnostic criteria or inclusion criteria; 2. Those with severe disturbance of consciousness, severe dementia, speech impairment, or other conditions preventing communication or description of symptoms; 3. Those with severe concomitant dysfunction of the heart, lung, liver, kidney, or other vital organs, or those in the acute phase of other serious diseases; 4. Those unable to comply with study requirements due to poor adherence; 5. Those allergic to moxibustion, or fearful of or intolerant to acupuncture and moxibustion; 6. Those currently participating in other clinical trials; 7. Those lost to follow-up during treatment. Anyone meeting any of the above criteria will be excluded.

Design outcomes

Primary

MeasureTime frame
Cerebral circulation indicators;NIHSS scale;ADL Scale (Modified Barthel Index);

Secondary

MeasureTime frame
Interleukin-1ß;Interleukin-6;Nuclear Factor Kappa B;Endothelin-1;Endothelial Nitric Oxide Synthase;

Countries

China

Contacts

Public ContactShen Cuicui

Wuxi No.2 People's Hospital

scc128@sina.com+86 150 5068 7936

Outcome results

None listed

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