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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03376048
Other study ID # KNUHC01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 20, 2017
Est. completion date December 30, 2019

Study information

Verified date February 2020
Source Kyungpook National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The TAP block is typically performed either with ultrasound guidance (TAP-US) or laparoscopic visualization (TAP-LAP): comparison between these two technics showed no differences in pain control and use of opioid analgesics.

The investigators hypothesize that WI is non-inferior to WI + TAP-block with respect to postoperative pain.


Description:

In colorectal surgery, laparoscopy and enhanced recovery after surgery (ERAS) programs have significantly improved the short-term outcomes (1). Although the laparoscopic approach reduces pain and recovery time, post-operative pain, nausea and vomiting still represent an issue. In order to reduce opioid related side effects, such as postoperative nausea and vomiting (PONV), constipation and prolonged post-operative ileus, non-opioid based multimodal analgesia have been recently introduced. Although epidural analgesia has gained good success, it does not seem to offer any additional clinical benefits to patients undergoing laparoscopic colorectal surgery compared to alternative analgesic technique within an ERAS program. Both local wound infiltration (WI) and TAP block are common techniques in multimodal postoperative pain treatment, and their association allows to achieve pain control despite a reduced use of opioid analgesics. Furthermore, in a recent single-blind prospective study TAP block resulted superior to wound infiltration alone. The TAP block is typically performed either with ultrasound guidance (TAP-US) or laparoscopic visualization (TAP-LAP): comparison between these two technics showed no differences in pain control and use of opioid analgesics.

The aim of this study is to compare WI + TAP-LAP versus WI alone. The investigators hypothesize that WI is non-inferior to WI + TAP-block with respect to postoperative pain.


Recruitment information / eligibility

Status Completed
Enrollment 108
Est. completion date December 30, 2019
Est. primary completion date April 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Aged 18-80 years, either sex

- Patients scheduled to undergo elective laparoscopic colorectal surgery under general anesthesia

- Willingness and ability to sign an informed consent document

Exclusion Criteria:

- Allergies to anesthetic or analgesic medications

- Contraindication to the use of locoregional anesthesia

- Chronic opioid use

- Coagulopathy, Impaired kidney function, uncontrolled diabetes, psychiatric disorders, severe cardiovascular impairment or chronic obstructive lung disease

- Necessity of major resection other than colorectal, palliative surgery

- BMI above 35 kg/m2

- American Society of Anesthesiologists (ASA) physical status above 3

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Wound infiltration plus TAP
TAP block: At the beginning of the main surgical procedure the surgeon will perform a TAP with ropivacaine infiltration, bilaterally in the anterior axillary line, between the costal margin and iliac crest in the intermuscular plane between the internal oblique and transversus abdominis muscles, the anesthesiologist under ultrasound guidance, the surgeon under laparoscopic guidance (two "pops" technique). Wound infiltration : Wound infiltration of ropivacaine will be performed by the surgeon before skin incision.
Wound infiltration
Wound infiltration of ropivacaine will be performed by the surgeon before skin incision.

Locations

Country Name City State
Italy University of Verona Hospital Trust and Colorectal Cancer Center Verona
Korea, Republic of Kyungpook National University Chilgok Hospital Daegu

Sponsors (1)

Lead Sponsor Collaborator
Kyungpook National University Hospital

Countries where clinical trial is conducted

Italy,  Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain numerical rating scale (NRS) Pain NRS during rest and cough
NRS scale 0-10: 0, "no pain"; 10, "worst pain imaginable"
within the first 6 hours after surgery
Secondary Pain NRS Pain NRS during rest and cough
NRS scale 0-10: 0, "no pain"; 10, "worst pain imaginable"
12, 24, 36, 48, 72 hour after surgery
Secondary Rescue opioid analgesic requirement Overall postoperative rescue of opioid analgesic requirement described by using the Defined Daily Dose postoperative day 0, 1, 2, 3
Secondary Postoperative nausea and vomiting scale PONV scores (assessed using a 0 - 2 categorical scale; no nausea/ nausea/ vomiting) 12, 24, 36, 48, 72 hour after surgery
Secondary Occurrence of prolonged post-operative ileus Occurrence of prolonged post-operative ileus (assessed using a 0 - 1 categorical scale; no ileus/ileus) 8 weeks after surgery
Secondary Time to first oral fluid intake Time to first oral fluid intake after surgery 8 weeks after surgery
Secondary Time to first oral soft diet Time to first oral soft diet after surgery 8 weeks after surgery
Secondary Length of hospital stay Length of hospital stay after admission 8 weeks after surgery
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