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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

West Raha, MBChB 07496833117
flicor.trial@imperial.ac.uk


Study Location:

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Be Part of Research - Trial Details - Feasibility Study of Lidocaine Infusion During Bowel Cancer Surgery for Cancer Outcome

Feasibility Study of Lidocaine Infusion During Bowel Cancer Surgery for Cancer Outcome

Not Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Colorectal Cancer
Quality of Life
Recurrent Cancer


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


This feasibility (small) study aims to see if it is possible to run a large study looking at the effect of lidocaine on large bowel cancer recurrence after surgery in the NHS hospitals.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Feb 2023 Sep 2024

Publications

"West R, Soo CP, Murphy J, Vizcaychipi MP, Ma D. A protocol for a pilot study to assess the feasibility of a randomised clinical trial of perioperative intravenous lidocaine on colorectal cancer outcome after surgery (FLICOR trial). BJA Open. 2023 Jun;6:100138. doi: 10.1016/j.bjao.2023.100138."; "37387798"

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : An intravenous bolus of 2% lidocaine will be administered following the induction of anaesthesia at 1.5mg/kg ideal body weight over 20 minutes followed by intravenous infusion of 1.5 mg/kg/hour ideal body weight with a maximum rate of 120mg/hour for 24 hours.

Intervention Arm Group : lidocaine;

Intervention Type : DRUG
Intervention Description : Administered as lidocaine

Intervention Arm Group : 0.9% sterile Sodium Chloride solution for injection;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Imperial College Healthcare NHS Trust
    London
  • Chelsea and Westminster Hospital NHS Foundation Trust
    London


The study is sponsored by Imperial College London




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Read full details for Trial ID: NCT05250791
Last updated 08 June 2023

This page is to help you find out about a research study and if you may be able to take part

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