Using electronic moxibustion to reduce pain and improve healing after brain surgery
Official title: Ffect of Electronic Moxibustion Apparatus on Pain Degree and Wound Healing of Patients After Craniocerebral Surgery
Run by The Fourth Affiliated Hospital of Zhejiang University School of Medicine · NCT06534710 · Data updated 2026-11-12
This study is testing if using an electronic moxibustion device can help reduce pain and improve healing for patients after brain surgery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 80 Years |
| Sex | All |
| Enrollment | 228 (estimated) |
| Sponsor | The Fourth Affiliated Hospital of Zhejiang University School of Medicine Academic / other |
| Locations | 1 site (Yiwu, Zhejiang) |
| Status | Recruiting |
| Started | September 1, 2024 |
| Main results expected | August 1, 2025 |
| Study ends | August 1, 2025 |
| Registry record updated | February 17, 2025 |
| Trial ID | NCT06534710 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults over 18 years old who are stable after craniocerebral surgery and have an expected hospitalization of more than three days.
✕Probably not a fit
Patients with serious organ dysfunction or those who are pregnant, lactating, or menstruating may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the effects of an electronic moxibustion apparatus on pain management and wound healing in patients who have undergone craniocerebral surgery. It aims to address the common issue of moderate to severe pain experienced by these patients, particularly within the first 24 hours post-surgery. By utilizing moxibustion, a traditional Chinese medicine technique, the study seeks to provide a non-pharmacological alternative to conventional analgesics, which often have undesirable side effects. The study will enroll patients who are stable after surgery and will monitor their pain levels and wound healing progress over time.
Why it matters
Potential benefit: If successful, this approach could significantly reduce pain and improve recovery outcomes for patients after craniocerebral surgery.
How similar studies have gone: While the use of moxibustion in pain management is established in traditional practices, this specific application in post-craniocerebral surgery patients is novel and has not been extensively tested in clinical settings.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients on the third day after craniocerebral surgery; ② Patients with vital signs and stable condition for more than 24 hours; (3) Meet the requirements of medical research ethics, and the subjects voluntarily join the clinical study and sign the informed consent; (4) The expected duration of hospitalization is \> 3 days; ⑤ Age \> 18 years old; Exclusion Criteria: ① Patients with serious heart, lung, liver, kidney and other vital organ dysfunction; ② Female patients in lactation period, menstrual period, pregnancy period or allergic constitution; Exclusion criteria: ① Patients or their family members should be excluded from this study in time due to disputes with the hospital during diagnosis or treatment (including requests for early transfer and termination of treatment).
Where it's running
-
the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine,Zhejiang University
Yiwu, Zhejiang, China Recruiting
Study contacts
- Study coordinator: guanhua hou
- Email: jigoulunli_zy4y@163.com
- Phone: +86 0579-89935052
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.