Multimodal Analgesia With Interfascial Continuous Wound Infiltration: A Randomized Clinical Trial

Sponsor
Hospital Galdakao-Usansolo (Other)
Overall Status
Completed
CT.gov ID
NCT02223533
Collaborator
(none)
110
1
2
24
4.6

Study Details

Study Description

Brief Summary

Objectives: For major laparoscopic surgery, as with open surgery a multimodal analgesia plan can help control postoperative pain. Placing a wound catheter intraoperatively following colon surgery could optimize the control of acute pain with less consumption of opioids and few adverse effects.

Methods: We conducted a prospective, randomized, study of 103 patients scheduled to undergo laparoscopic colon surgery for cancer in Galdakao-Usansolo Hospital.

Patients were recruited and randomly allocated to wound catheter placement plus standard postoperative analgesia or standard postoperative analgesia alone. A physician from the acute pain management unit monitored all patients for at multiple points over the first 48 hours after surgery. The primary outcome variables were verbal numeric pain scale (NRS) scores and amount of intravenous morphine used via patient controlled infusion.

Condition or Disease Intervention/Treatment Phase
Phase 4

Study Design

Study Type:
Interventional
Actual Enrollment :
110 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Treatment
Official Title:
Multimodal Analgesia With Interfascial Continuous Wound Infiltration of a Local Anaesthetic vs Intravenous Opioids After Laparoscopic Colon Surgery: A Randomized Clinical Trial.
Study Start Date :
Jan 1, 2012
Actual Primary Completion Date :
Jan 1, 2013
Actual Study Completion Date :
Jan 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Wound catheter

analgesia with wound catheter after colon surgery

Device: 19Gx500-mm Pajunk InfiltraLong® catheter
Before completing the surgery, the surgical team inserted a 19Gx500-mm Pajunk InfiltraLong® catheter with multiple perforations in the last few centimeters before the tip to allow for local anesthetic administration.

Active Comparator: morphine

analgesia with morphine after colon surgery

Drug: morphine
After the intervention patients had access to intravenous morphine via a patient-controlled analgesia

Outcome Measures

Primary Outcome Measures

  1. Assessment of Numerical Rating Pain Scale (NRS) after laparoscopic colon surgery using interfascial continuous wound infiltration [Over the 48 hours after laparoscopic colon surgery]

    Numerical Rating Pain Scale was used to measure the after-intervention Pain. This scale is widely used and shows good correlation with the Visual Analogue scale, specifically in the case of elderly individuals. Compared to other scales, it has low error rates and high validity. This score was assessed in all the participants.

  2. Assessment of intravenous morphine consumption after laparoscopic colon surgery [Over the 48 hours after laparoscopic colon surgery]

    Intravenous morphine consumption was administrated via patient-controlled analgesia device. The consumption was evaluated in all participants in the study at the following measurement points: at 30 min, 2h, 8h, 24h, and 48h after the intervention.

Secondary Outcome Measures

  1. Complications related to intravenous morphine consumption [Over the 48 hours after laparoscopic colon surgery]

    Complications related to intravenous morphine consumption were measured: nausea, vomiting and pruritus throughout the treatment period. Paralytic ileus awas measured 24h after surgery. This was assessed for all patients. Moreover, especially for patients belonging to the experimental group, potential adverse effects from placement of the wound catheter such as infection or haematoma at the surgical site or potential toxicity of local anesthetic (e.g., tinnitus, obnubilation) were recorded.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients were eligible for the study if they were aged 18 years or older, with an American Society of Anesthesiologists (ASA) 14 grade of I to IV (anaesthetic risk), were scheduled to undergo laparoscopic colon surgery, and voluntarily agreed to participate by signing an informed consent form.
Exclusion Criteria:
  • Patients were excluded if they were allergic to amides or pyrazolones, were likely to require conversion to open surgery with laparotomy, were long-term users of opioids, required emergency surgery, were unable to participate due to cognitive deterioration, or declined to participate in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital de GAldakao-Usansolo Usansolo Biscay Spain 48960

Sponsors and Collaborators

  • Hospital Galdakao-Usansolo

Investigators

  • Principal Investigator: Sorkunde Telletxea, MD, PhD, Hospital Galdakao-Usansolo

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sorkunde Telletxea, MD, PhD, MD, PhD, Hospital Galdakao-Usansolo
ClinicalTrials.gov Identifier:
NCT02223533
Other Study ID Numbers:
  • sork-2011111058
First Posted:
Aug 22, 2014
Last Update Posted:
Aug 22, 2014
Last Verified:
Aug 1, 2014
Keywords provided by Sorkunde Telletxea, MD, PhD, MD, PhD, Hospital Galdakao-Usansolo
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 22, 2014