Transversus abdominis plane blok, continous systemic administration of lidocain and patient controlled intravenous morphine - 3 methods for postoperative pain control after laparoscopic colorectal surgery: a randomised comparative trial

Phase 1

• Conditions: postoperative pain; MedDRA version: 17.1Level: LLTClassification code 10036236Term: Postoperative pain reliefSystem Organ Class: 100000004865; Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]

• Registration Number: EUCTR2014-001499-73-BE
• Lead Sponsor: niversity Hospitals Leuven

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2014-06-13
• Study Completion: 2017-01-16
• Last Update Posted: 5 April 2021

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 125

Inclusion Criteria

ASA 1,2 &3
laparoscopic colorectal surgery
patients between 18 and 75 years of age
written informed consent
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 85
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 40

Exclusion Criteria

allergic to lidocain
chronic use of opiods
liver insufficiency (bili total >= 2 mg/dl)
renal insufficiency (eGFR<= 60 ml/min/1.73m**2)
epilepsy
morbide obesity
sleep apneu
cardiac dysrhythmia
mental retardation

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified