Overview
Bilateral Transversus Abdominis Plane Block Versus Atracurium During Laparoscopic Gynecology Procedures.
Status:
Completed
Completed
Trial end date:
2015-10-31
2015-10-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
A monocentric, prospective, randomized controlled trial, including patients proposed for a laparoscopic gynecologic surgery comparing the muscular relaxing effect of a bilateral ultrasound-guided Transversus Abdominis Plane block to usual neuromuscular blockade agent (Atracurium)Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University Tunis El ManarTreatments:
Atracurium
Neuromuscular Blocking Agents
Criteria
Inclusion Criteria:- American Association of anesthesiologists' class I to III (ASA I to ASA III)
- undergoing laparoscopic gynecologic procedures
Non inclusion Criteria:
- patients' refusal to be part of the study
- ASA IV and higher
- known allergic history to Propofol or any of its components (eggs, soya and beans,
etc.), suxamethonium, Fentanyl or Atracurium.
- Patients who presents any regional anesthesia contraindication as clotting disorders,
injection site infection and allergy to local anesthetics
- Psychiatric and neurologic disorders and the inability to understand pain scores and
the study protocol
Exclusion Criteria:
- unsuccessful TAP block
- Observed anesthesia or surgical incident which requires the end of the ongoing
procedure or the conversion to laparotomy