Parkinson’s Disease – INT-001
The objective of this clinical trial is to explore the analgesic effect of intradermal needle therapy on patients after gastric endoscopic submucosal dissection; analyze factors related to postoperative pain in gastric endoscopic submucosal dissection (ESD) patients, and evaluate the safety of intradermal needle therapy.
Inclusion Criteria:
- Meet the surgical indications for gastric endoscopic submucosal dissection;
- All patients signed a written “Surgical Consent Form” before surgery;
- Complete clinical data;
- Informed consent and participation in this study.
- Other criteria may apply
Complete the form and our team will reach out soon to help determine your eligibility.