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Clinical Trials/ITMCTR2100004607
ITMCTR2100004607
Recruiting
Phase 1

Clinical study on the effect of electroacupuncture on blood flow of internal carotid artery in patients with laparoscopic gallbladder surgery

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine0 sitesTBD
ConditionsGallstone

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Gallstone
Sponsor
Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Sponsor
Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine

Eligibility Criteria

Inclusion Criteria

  • 1\. Elective laparoscopic cholecystectomy is performed, and the preoperative patient classification (ASA classification) of the American Society of Anesthesiologists is I\-III;
  • 2\. Age \>\= 18 years old and \<\= 75 years old, no gender limit;
  • 3\. Body mass index 18\-32kg/m2 (body mass index BMI \= weight (kg) / height 2 (m2\));
  • 4\. Understand and agree to participate in this study and sign an informed consent form.

Exclusion Criteria

  • 1\.Known transient ischemic attack, subarachnoid hemorrhage and cerebral hemorrhage, cerebral infarction, brain tumor, cerebrovascular malformation, cerebral arteritis, brain trauma and other brain diseases.
  • 2\.Those with severe liver and kidney function damage (ALT, AST, BUN, Cr exceeding 1\.5 times the normal value).
  • 3\.Myelitis, spinal cord demyelination, spinal cord compression, spinal cord tumors and other central nervous system diseases.
  • 4\.Patients who have undergone surgery on acupoints and meridians.
  • 5\.Patients with local skin infections at acupoints.
  • 6\.Those who have participated in or are participating in other clinical trials within 4 weeks before enrollment.

Outcomes

Primary Outcomes

Not specified

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