Effects of Different Types of Perioperative Analgesia on Minimal Residual Disease Development After Colon Cancer Surgery
Colon Cancer, Minimal Residual Disease
About this trial
This is an interventional treatment trial for Colon Cancer focused on measuring perioperative analgesia, minimal residual disease, cancer recurrence, epidural, morphine, piritramide, colon, cancer, circulating cancer cells, colon cancer surgery
Eligibility Criteria
Inclusion Criteria:
- Patients undergoing open radical surgery for colon cancer (without known extension beyond colon)
- Age over 18 years
- Written informed consent
Exclusion Criteria:
- Allergy or intolerance of morphine, piritramide, marcaine, sufentanil or volatile anesthetics
- History of colon cancer resection
- Other cancer present (apart from those in complete long-term remission for minimum 6 months)
- Chronic opioid medication and/or opioid administration 7 days or less prior to surgery
- Any contraindication to thoracic epidural anesthesia/analgesia
- Systemic therapy with immunosuppressive drugs or corticoids (apart from topical and inhalational)
- Any surgery within the last 30 days (apart from minor day-case procedures)  - Chronic or acute infectious disease, particularly hepatitis, AIDS, tuberculosis
Sites / Locations
- Brno University Hospital
- T. Bata Regional Hospital Zlin
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Active Comparator
Epidural
Piritramide
Morphine
Patients will receive perioperative epidural analgesia. Drugs: bupivacaine 1.25 mg/ml and sufentanil 0.5 mcg/ml Form and frequency: continuous infusion Dosage: 4 - 14 ml/h with boluses 2 - 4 ml based on pain assessment Duration: as long as required
Patients will receive postoperative analgesia with piritramide. Drugs: piritramide 1.0 mg/ml Form and frequency: continuous infusion Dosage: 0 - 4 ml/h with boluses 2 - 4 ml based on pain assessment Duration: as long as required
Patients will receive postoperative analgesia with morphine. Drugs: morphine 1.0 mg/ml Form and frequency: continuous infusion Dosage: 0 - 4 ml/h with boluses 2 - 4 ml based on pain assessment Duration: as long as required