Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03638401
Other study ID # RL14/11048
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 3, 2014
Est. completion date October 5, 2015

Study information

Verified date August 2018
Source The Leeds Teaching Hospitals NHS Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Good postoperative pain control after any major surgery allows early mobilization, minimises postoperative complications and reduces patient distress. Multiple different methods of delivering analgesia have been described.

This study aims to compare postoperative pain control between patients with epidural analgesia versus the combination of continuous infiltration of local anaesthetic with wound catheters, TAP block and IV PCA with opiate analgesia following open liver resection. The investigators expect that pain control will be similar between the two groups but that the utilization of wound catheters will confer benefit due to the lack of systemic side effects associated with epidural analgesia


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date October 5, 2015
Est. primary completion date October 5, 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

- All adult patients scheduled to undergo an open liver resection at this hospital will be eligible to participate.

Exclusion Criteria:

- Patients with a contraindication to either epidural or wound catheter

- Inability to give written, informed consent

- Aged less than 18 years old

- Liver resection combined with a secondary surgical procedure

- Body mass index of <18 or >40

- Pregnancy or lactation

- A history of chronic pain requiring regular opioid analgesia

- Prisoners

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
This arm will received perioperative transversus abdominis plane (TAP) block followed by continuous infusion of local anaestheic by wound catheters and an IV morphine PCA.
This arm will received perioperative transversus abdominis plane (TAP) block followed by continuous infusion of local anaestheic by wound catheters and an IV morphine PCA.

Locations

Country Name City State
United Kingdom Leeds Teaching Hospitals NHS Trust Leeds

Sponsors (1)

Lead Sponsor Collaborator
The Leeds Teaching Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary The length of hospital stay following open liver resection 6 months (or length of the study)