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Local Anesthesia Versus Saline Serum in Surgical Incision of Colorectal or Hepatic Surgery (CATROP-2007)

Primary Purpose

Postoperative Pain, Surgery, Postoperative Complications

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
ropivacaine
saline solution
Sponsored by
Hospital Universitari de Bellvitge
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postoperative Pain focused on measuring postoperative pain, wound infusion, local anesthesia

Eligibility Criteria

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

Inclusion Criteria:

  • ASA I-III
  • Undergoing scheduled colorectal cancer and hepatic surgery
  • Patients must be able to understand the PCA (the self administration system)

Exclusion Criteria:

  • Background of allergic reaction or contraindication for local anesthesia or non steroid anti-inflammatory drugs.
  • Patient with epidural catheter or receiving combined analgesia during surgery (age above 80, moderate-severe respiratory dysfunction, patients who prior presented complex postoperative pain management.
  • Emergency surgery
  • Patients with risk of hepatic insufficiency (Klatskin's tumor, extended right hepatectomy, right hepatectomy in patients with steatosis, hepatic resection in patients over 70 years of age who have been given chemotherapy).
  • Inflammatory bowel disease: ulcerative colitis, Crohn's disease.
  • Major psychiatric condition.
  • Patients with active drug addiction or on chronic treatment with opiates.
  • Morbid obesity (BMI > 35 kg/m2)
  • Patients with heart disease (myocardiopathy, conduction alterations, antiarrhythmic treatment) and severe liver disease (alteration synthesis, histolysis and or cholestasis).
  • Patients with kidney failure.
  • Patients treated with fluvoxamine (antidepressant) and enoxacin (antibiotic) both are potent inhibitors of CYPIA2.
  • Septic patients
  • Patients that do not wish to participate.

Sites / Locations

  • Anesthesiology Service of Univeritary Hospital of Bellvitge

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Ropivacaine

saline solution

Arm Description

After a bolus administration of Ropivacaine a perfusion ot the same anesthetic is initiated through an elastomeric wound during 48 hours

After a bolus administration of saline solution a perfusion ot saline solution is initiated through an elastomeric wound during 48 hours

Outcomes

Primary Outcome Measures

Mg of Morphine Consumption During 48 Hours Administered by Patient Controlled Analgesia System

Secondary Outcome Measures

Intensity of Pain Measured by Verbal Pain Scale.
Verbal pain scale is a numeric measure of intensity pain, values range from 0 (no pain) to 10 (excruciating pain), Each patient rate the paín that feel with a number from 0 to 10.
Time Spent Sitting in a Chair, Deambulation, Solid Ingestion.
Secondary Effects Due to Morphine: Nausea and Vomiting
Local Reaction in the Wound and Insertion Point of the Catheter (Inflammation Signs and Infection)
Contamination of the Catheter (Microbiologist Analysis)

Full Information

First Posted
January 11, 2010
Last Updated
February 23, 2017
Sponsor
Hospital Universitari de Bellvitge
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1. Study Identification

Unique Protocol Identification Number
NCT01075646
Brief Title
Local Anesthesia Versus Saline Serum in Surgical Incision of Colorectal or Hepatic Surgery
Acronym
CATROP-2007
Official Title
Randomised and Double-blind Clinical Trial on Post-operative Analgesic Efficacy in Colorectal Surgery and Hepatic Surgery With Continuous Infusion of Local Anesthesia vs Saline Serum in the Surgical Incision.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
March 2009 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
June 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitari de Bellvitge

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether a continuous infusion of local anesthesia with a catheter in the surgical wound reduces patient consumption of opiates by 30% in the 48-hour postoperative period following surgery for colorectal neoplasm and hepatic surgery versus the continuous infusion of physiological serum.
Detailed Description
Postoperative analgesia in major abdominal surgery is managed with intravenous PCA (patient controlled analgesia) with morphine associated to non-steroidal anti-inflammatories drugs (NSAD) and paracetamol in the first 48 hours of the postoperative phase. With this multimodal approach patients undergoing colorectal surgery have a median pain score on the verbal scale (0-10) of 3 (range 0-8) with a mean of morphine consumption of 54 mg (SD 24 mg) and patients undergoing hepatic surgery have a median pain score of 2(range 0-7) with a mean of morphine consumption of 28 mg (SD 17 mg). Although opiates are very potent analgesics they also produce side effects and numerous studies have demonstrated a significant reduction in morbidity when patients received lower dose of opiates during anesthesia and in postoperative period. Continuous infusion of local anesthetics in the surgical wound has been used for pain control in different types of surgeries. However, controversial reports has been reported in abdominal surgery. We are conducting prospective, randomised and double-blind placebo control trials in two surgical models (colo-rectal oncologic surgery and hepatic resection) using continuous perfusion of ropivacaine 0.38% in the surgical wound versus saline. Anesthetic protocol is the same for all patients. Patients undergoing colo-rectal surgery can be operated either in laparotomy or laparoscopic technique therefore patients are stratified into four groups once surgical closure has begun: Group A1 ropivacaine and laparotomy Group A2 ropivacaine and laparoscopy Group B1 saline and laparotomy Group B2 saline and laparoscopy In the preanesthesia visit patients who match inclusion criteria are invited to participate in the study and they signed the informed consent. When the patient is in the theatre a nurse not involved in the management of patients opens a closed envelope which indicates the solution to be prepared according to the assigned group. The surgeon inserts a multiperforated catheter at the subfascial level of surgical wound , just below the suture of the muscular fascia (between the peritoneum and the muscular fascia) and after that surgeons finish the subcutaneous plane and the skin. After the closure a bolus of 5 ml (laparoscopy colon surgery)or 10 ml (laparotomy colon and hepatic surgery) of the solution is given through the catheter and subsequently an elastomer filled with ropivacaine or saline is connected. The catheter is fixed to the skin with steri-strip and sterile dressing. During the procedure we administer in a protocol basis the NSAD and thirty minutes before the end of the surgery we administer morphine. In the postoperative period the patient receives a NSAD regime and a PCA morphine treatment. The catheter is withdrawn after 48 hours and also the PCA and the analgesic treatment is with NSAD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Pain, Surgery, Postoperative Complications
Keywords
postoperative pain, wound infusion, local anesthesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
225 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ropivacaine
Arm Type
Experimental
Arm Description
After a bolus administration of Ropivacaine a perfusion ot the same anesthetic is initiated through an elastomeric wound during 48 hours
Arm Title
saline solution
Arm Type
Placebo Comparator
Arm Description
After a bolus administration of saline solution a perfusion ot saline solution is initiated through an elastomeric wound during 48 hours
Intervention Type
Drug
Intervention Name(s)
ropivacaine
Other Intervention Name(s)
(wound infusion ropivacaine)
Intervention Description
Laparotomy of colorectal surgery: 10 ml bolus ropivacaine 0,75% + infusion with elastomeric pump with ropivacaine 0,38% at a 5ml/h. Laparoscopy of colorectal surgery: 5 ml bolus ropivacaine 0,75% + infusion with elastomeric pump with ropivacaine 0,38% at a 2 ml/h. Hepatic surgery: 10 ml de ropivacaine 0,45% + infusion with elastomeric pump with ropivacaine 0,23 at a 5ml/h.
Intervention Type
Drug
Intervention Name(s)
saline solution
Other Intervention Name(s)
wound infusion saline solution
Intervention Description
Laparotomy of colorectal surgery: 10 ml bolus saline solution 0.9% + infusion with elastomeric pump with saline solution 0.9% at a 5ml/h. Laparoscopy of colorectal surgery: 10 ml bolus saline solution 0.9% + infusion with elastomeric pump with saline solution 0.9% at a 2 ml/h. Hepatic surgery: 10 ml de saline solution 0.9% + infusion with elastomeric pump with saline solution 0.9% at a 5ml/h
Primary Outcome Measure Information:
Title
Mg of Morphine Consumption During 48 Hours Administered by Patient Controlled Analgesia System
Time Frame
48 hours
Secondary Outcome Measure Information:
Title
Intensity of Pain Measured by Verbal Pain Scale.
Description
Verbal pain scale is a numeric measure of intensity pain, values range from 0 (no pain) to 10 (excruciating pain), Each patient rate the paín that feel with a number from 0 to 10.
Time Frame
At interval periods during 48 hours
Title
Time Spent Sitting in a Chair, Deambulation, Solid Ingestion.
Time Frame
7 Days (from Day 8-15)
Title
Secondary Effects Due to Morphine: Nausea and Vomiting
Time Frame
during 48 hours
Title
Local Reaction in the Wound and Insertion Point of the Catheter (Inflammation Signs and Infection)
Time Frame
During 8-15 days
Title
Contamination of the Catheter (Microbiologist Analysis)
Time Frame
at 48 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ASA I-III Undergoing scheduled colorectal cancer and hepatic surgery Patients must be able to understand the PCA (the self administration system) Exclusion Criteria: Background of allergic reaction or contraindication for local anesthesia or non steroid anti-inflammatory drugs. Patient with epidural catheter or receiving combined analgesia during surgery (age above 80, moderate-severe respiratory dysfunction, patients who prior presented complex postoperative pain management. Emergency surgery Patients with risk of hepatic insufficiency (Klatskin's tumor, extended right hepatectomy, right hepatectomy in patients with steatosis, hepatic resection in patients over 70 years of age who have been given chemotherapy). Inflammatory bowel disease: ulcerative colitis, Crohn's disease. Major psychiatric condition. Patients with active drug addiction or on chronic treatment with opiates. Morbid obesity (BMI > 35 kg/m2) Patients with heart disease (myocardiopathy, conduction alterations, antiarrhythmic treatment) and severe liver disease (alteration synthesis, histolysis and or cholestasis). Patients with kidney failure. Patients treated with fluvoxamine (antidepressant) and enoxacin (antibiotic) both are potent inhibitors of CYPIA2. Septic patients Patients that do not wish to participate.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antònia Dalmau Llitjós, Physical D
Organizational Affiliation
Univeritary Hospital of Bellvitge. IDIBELL
Official's Role
Study Director
Facility Information:
Facility Name
Anesthesiology Service of Univeritary Hospital of Bellvitge
City
Hospitalet . Barcelona
State/Province
Barcelona
ZIP/Postal Code
08907
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
17116561
Citation
Liu SS, Richman JM, Thirlby RC, Wu CL. Efficacy of continuous wound catheters delivering local anesthetic for postoperative analgesia: a quantitative and qualitative systematic review of randomized controlled trials. J Am Coll Surg. 2006 Dec;203(6):914-32. doi: 10.1016/j.jamcollsurg.2006.08.007. Epub 2006 Oct 25. No abstract available.
Results Reference
background
PubMed Identifier
17721249
Citation
Beaussier M, El'Ayoubi H, Schiffer E, Rollin M, Parc Y, Mazoit JX, Azizi L, Gervaz P, Rohr S, Biermann C, Lienhart A, Eledjam JJ. Continuous preperitoneal infusion of ropivacaine provides effective analgesia and accelerates recovery after colorectal surgery: a randomized, double-blind, placebo-controlled study. Anesthesiology. 2007 Sep;107(3):461-8. doi: 10.1097/01.anes.0000278903.91986.19.
Results Reference
background
PubMed Identifier
16040091
Citation
Wu CL, Partin AW, Rowlingson AJ, Kalish MA, Walsh PC, Fleisher LA. Efficacy of continuous local anesthetic infusion for postoperative pain after radical retropubic prostatectomy. Urology. 2005 Aug;66(2):366-70. doi: 10.1016/j.urology.2005.02.030.
Results Reference
background
PubMed Identifier
15385371
Citation
Gupta A, Perniola A, Axelsson K, Thorn SE, Crafoord K, Rawal N. Postoperative pain after abdominal hysterectomy: a double-blind comparison between placebo and local anesthetic infused intraperitoneally. Anesth Analg. 2004 Oct;99(4):1173-1179. doi: 10.1213/01.ANE.0000130260.24433.A2.
Results Reference
background
PubMed Identifier
11473884
Citation
Zohar E, Fredman B, Phillipov A, Jedeikin R, Shapiro A. The analgesic efficacy of patient-controlled bupivacaine wound instillation after total abdominal hysterectomy with bilateral salpingo-oophorectomy. Anesth Analg. 2001 Aug;93(2):482-7, 4th contents page. doi: 10.1097/00000539-200108000-00048.
Results Reference
background
PubMed Identifier
11133625
Citation
Fredman B, Zohar E, Tarabykin A, Shapiro A, Mayo A, Klein E, Jedeikin R. Bupivacaine wound instillation via an electronic patient-controlled analgesia device and a double-catheter system does not decrease postoperative pain or opioid requirements after major abdominal surgery. Anesth Analg. 2001 Jan;92(1):189-93. doi: 10.1097/00000539-200101000-00036.
Results Reference
background
PubMed Identifier
2604350
Citation
Chester JF, Ravindranath K, White BD, Shanahan D, Taylor RS, Lloyd-Williams K. Wound perfusion with bupivacaine: objective evidence for efficacy in postoperative pain relief. Ann R Coll Surg Engl. 1989 Nov;71(6):394-6.
Results Reference
background
PubMed Identifier
16427556
Citation
Baig MK, Zmora O, Derdemezi J, Weiss EG, Nogueras JJ, Wexner SD. Use of the ON-Q pain management system is associated with decreased postoperative analgesic requirement: double blind randomized placebo pilot study. J Am Coll Surg. 2006 Feb;202(2):297-305. doi: 10.1016/j.jamcollsurg.2005.10.022.
Results Reference
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Local Anesthesia Versus Saline Serum in Surgical Incision of Colorectal or Hepatic Surgery

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