Opioid Use Clinical Trial
Official title:
Effects of Cranial Electrotherapy Stimulation on Anesthetics Consumption, Perioperative Cytokines Response, and Postoperative Pain in Patients Undergoing Colonic Surgery
Cranial electrotherapy stimulation (CES) is a non-invasive intervention to treat anxiety, depression, insomnia, and pain. But clinical studies and applications of CES in relation to acute postoperative pain are few. tThe investigators investigate a double-blind, randomized controlled trial to figure out if intraoperative CES could decrease dosage of intraoperative anesthetics and patient-controlled analgesia (PCA) consumption in patients undergoing colon cancer surgery.
Status | Recruiting |
Enrollment | 80 |
Est. completion date | December 31, 2020 |
Est. primary completion date | December 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Patients undergoing colon cancer surgery Exclusion Criteria: - presence of an implantable device (e.g., pacemaker) - pregnancy - having a known mental illness (e.g., schizophrenia, mood disorder, bipolar disorder, etc. - cancer of the head and neck or brain tumor or brain metastasis - having delirium |
Country | Name | City | State |
---|---|---|---|
Taiwan | TriService General Hospital | Taipei |
Lead Sponsor | Collaborator |
---|---|
Tri-Service General Hospital |
Taiwan,
Lee SH, Kim WY, Lee CH, Min TJ, Lee YS, Kim JH, Park YC. Effects of cranial electrotherapy stimulation on preoperative anxiety, pain and endocrine response. J Int Med Res. 2013 Dec;41(6):1788-95. doi: 10.1177/0300060513500749. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | dosage of intraoperative anesthetics | The consumption of total amount of supplemental analgesics administered during colon cancer surgery | during surgery | |
Primary | Rescue analgesics | The consumption of total amount of rescue analgesics administered after colon cancer surgery | from the end of the surgery to postoperative 72 hours | |
Primary | Differences in Pain Intensity Between CES intervention and the control group | Pain assessment of NRS pain intensity scores and patient satisfaction assessed by the NRS through end of surgery to postoperative 72 hours | from the end of the surgery to postoperative 72 hours | |
Secondary | dosage of patient-controlled analgesia (PCA) consumption | postoperative PCA consumption | from the end of the surgery to postoperative 72 hours | |
Secondary | serum concentration of serum cytokine | proinflammatory and antiinflammatory cytokines (IL-1a, IL-2, IL-6, IL-7, TNF-a, IL-4, IL-10, IL-10, IL-1, TGF-b) | from the beginning of the surgery to postoperative 72 hours | |
Secondary | Number of Participants with CES and control groups | patient characteristics | during surgery |
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