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Spots Global Cancer Trial Database for Optimal Peripheral Nerve Block After Minimally Invasive Colon Surgery

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Trial Identification

Brief Title: Optimal Peripheral Nerve Block After Minimally Invasive Colon Surgery

Official Title: Laparoscopic vs Ultrasound-Guided Transversus Abdominis Plane Block in Minimally Invasive Colon Surgery: A Randomized Controlled Multicentre Clinical Trial

Study ID: NCT04311099

Study Description

Brief Summary: The purpose of the trial is to identify the "most simple non-inferior of three different methods", placebo, laparoscopic assisted transverse abdominal plane block (L-TAP) and ultrasound guided TAP block (US-TAP), using postoperative opioid consumption as a measure of efficacy in patients undergoing elective minimally invasive colon surgery in an ERAS setting. Postoperative pain scores and length of stay (LOS) will also be measured. The simplicity of the three methods is ranked as: 1) placebo, 2) L-TAP and 3) US-TAP.

Detailed Description: Introducing laparoscopy in colorectal surgery and optimizing the postoperative care using the standardized protocols of enhanced recovery after surgery (ERAS) have significantly improved patient outcomes and LOS. Better pain management has the potential to further improve these outcomes. Since the introduction of ultrasound-guided abdominal wall blocks, much research has been done in that field, but no consensus has been reached concerning the optimal block technique; where to and when to inject the block, or which drug to use. Newly published randomized controlled trials show interesting results regarding the L-TAP which has several advantages to the US-TAP, including the ease of performance, less dependency on specialized skills or equipment and avoidance of intraperitoneal infiltration. but these results need to be solidified with multicentre trials. Besides optimizing postoperative pain management, better block techniques could potentially decrease LOS in patients after minimally invasive colorectal surgery.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Sydvestjysk Sygehus, Esbjerg, , Denmark

Regionshospitalet Herning, Herning, , Denmark

Copenhagen University Hospital - North Zealand, Hillerød, , Denmark

Copenhagen University Hospital - Hvidovre, Hvidovre, , Denmark

Regionshospitalet Viborg, Viborg, , Denmark

Contact Details

Name: Claus A Bertelsen, PhD

Affiliation: Copenhagen University Hospital - North Zealand

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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