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Epidural Versus Patient-controlled Analgesia for Reduction in Long-term Mortality Following Colorectal Cancer Surgery (EPICOL)

Primary Purpose

Colorectal Cancer, Pain, Other Complications

Status
Terminated
Phase
Phase 3
Locations
Sweden
Study Type
Interventional
Intervention
Ropivacaine + opioid epidurally
Morphine
Sponsored by
Örebro University, Sweden
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Cancer focused on measuring Epidural analgesia, Patient controlled analgesia, Colorectal cancer, Morbidity, Mortality

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ASA status 1-3
  • Age group 40-80 years old
  • Undergoing elective surgery for colorectal cancer

Exclusion Criteria:

  • All contraindications to epidural analgesia
  • Chronic opiate medication/drug abuse
  • Allergy to morphine

Sites / Locations

  • University Hospital
  • University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Epidural anesthesia and analgesia

Patient controlled analgesia

Arm Description

Outcomes

Primary Outcome Measures

Long-term (up to 5 yrs) all-cause mortality
Cancer specific as well as all-cause mortality would be recorded.

Secondary Outcome Measures

Cancer recurrence detected by MRI; perioperative complications
All complications during the perioperative period including cancer recurrence detected by MRI examination once each year would be recorded.

Full Information

First Posted
March 17, 2011
Last Updated
February 15, 2021
Sponsor
Örebro University, Sweden
Collaborators
University Hospital, Linkoeping
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1. Study Identification

Unique Protocol Identification Number
NCT01318161
Brief Title
Epidural Versus Patient-controlled Analgesia for Reduction in Long-term Mortality Following Colorectal Cancer Surgery
Acronym
EPICOL
Official Title
Epidural or Patient-controlled Analgesia for Colorectal Cancer Surgery. Long-term Outcomes.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Terminated
Why Stopped
Difficulty in recruiting
Study Start Date
March 2011 (undefined)
Primary Completion Date
December 2020 (Actual)
Study Completion Date
January 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Örebro University, Sweden
Collaborators
University Hospital, Linkoeping

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Colorectal cancer is one of the most common cancers in the industrialized world (12% of all cancers). In Sweden, 6000 new cases of colorectal cancer are reported each year, and almost half of these cases result in death. Several recently published retrospective studies show that regional anaesthesia (RA) can reduce cancer-related mortality following surgical treatment of colorectal, breast and prostate cancers and malignant melanoma. If these results are true, then the choice of perioperative pain management is as beneficial, or even better, than the current oncological therapies. This theory needs to be investigated in a prospective, randomized and controlled trail.
Detailed Description
An application was sent to the Regional Ethics Committee at the Linköping University Hospital and the study was approved recently. Informed consent will be obtained from 300 patients (ASA status 1-3) in the age group 40-80 years who are undergoing elective surgery for colorectal cancer. The exact type of cancer, its staging, degree of spread to proximal or distant sites and the pathologic type of cancer will be recorded. Patients on chronic narcotic analgesic medication, those with known immunologic diseases, those with known allergy to LA and those where epidural catheter placement is contraindicated will be excluded. This study will be a multi-centre study in Central Sweden. Patients will be randomized to one of two groups according to a computer-generated random number: Group E - Epidural anaesthesia (EDA) or Group P - Patient-controlled analgesia (PCA). Anaesthesia and surgery will be standardized, other than for group randomization. Surgical management of patients in the hospitals will also be standardized. Postoperative parameters will include pain intensity, rescue analgesic (morphine) consumption, surgical complications (e.g., re-operation, surgical site infection, or bleeding), other perioperative complications (e.g., deep vein thrombosis, cardiac complications, or chest infections), cancer recurrence diagnosed by CT or MRI (done yearly over 5 years) and mortality, both cancer-related and all-cause mortality. In addition, blood will be taken preoperatively for analysis of the following inflammatory and immunological markers: VEGF will be determined in peritoneal fluid and in serum during surgery. HIF-1A will be determined by immunohistochemistry and microRNA measurements in normal and neoplastic colonic mucosa. In addition, the microRNA mi21 will be analyzed in by quantitative reverse transcriptase-PCR in colon adenocarcinomas and adjacent non-cancerous tissues. The CTC in whole blood (in 5-7.5 ml) will be measured with the CellSearch System, according to the manufacturer´s instructions, and the Cell Tracks Analyzer II (Cristofanilli M et al. N Engl J Med 2004:351:781-91). Inflammatory mediator assay-ELISA Patient serum or EDTA/Heparin plasma will be assessed for cytokine levels by a Luminex multiplex assay (Human Inflammation 12-Plex kit; GM.CSF, IFN-g, IL-1b, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12, TNF-a and VEGF from R&D system) and PGE2 levels will be measured by an ELISA kit from Cayman Chemicals Company. In addition, markers of systemic inflammatory response, including CRP, white blood cell count, differential count and total platelet count, will also be measured before and after surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Pain, Other Complications
Keywords
Epidural analgesia, Patient controlled analgesia, Colorectal cancer, Morbidity, Mortality

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
221 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Epidural anesthesia and analgesia
Arm Type
Experimental
Arm Title
Patient controlled analgesia
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Ropivacaine + opioid epidurally
Intervention Description
Epidural analgesia with local anesthetic + opioid
Intervention Type
Drug
Intervention Name(s)
Morphine
Intervention Description
Morphine via PCA pump
Primary Outcome Measure Information:
Title
Long-term (up to 5 yrs) all-cause mortality
Description
Cancer specific as well as all-cause mortality would be recorded.
Time Frame
7 years from start of enrollment
Secondary Outcome Measure Information:
Title
Cancer recurrence detected by MRI; perioperative complications
Description
All complications during the perioperative period including cancer recurrence detected by MRI examination once each year would be recorded.
Time Frame
7 years following start of enrollment
Other Pre-specified Outcome Measures:
Title
Inflammation
Description
Perioperative cytokine concentration in blood assessed between randomised groups as well as surgical technique after 100 recruited patients
Time Frame
0-5 days
Title
Postoperative pain and early recovery
Description
Aspects of early postoperative recovery until discharge would be measured after 200 recruited patients between randomised groups as well as surgical techniques
Time Frame
0 - 7 days postoperatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ASA status 1-3 Age group 40-80 years old Undergoing elective surgery for colorectal cancer Exclusion Criteria: All contraindications to epidural analgesia Chronic opiate medication/drug abuse Allergy to morphine
Facility Information:
Facility Name
University Hospital
City
Linköping
ZIP/Postal Code
581 85
Country
Sweden
Facility Name
University Hospital
City
Örebro
ZIP/Postal Code
701 85
Country
Sweden

12. IPD Sharing Statement

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Epidural Versus Patient-controlled Analgesia for Reduction in Long-term Mortality Following Colorectal Cancer Surgery

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