Posterior Transversus Abdominis Plane Block Combined With Sacral Multifidus Plane Block Versus Posterior Transversus Abdominis Plane Block for Laparoscopic Colorectal Surgery
Recruiting
N/AInterventional Study
AnesthesiaPosterior Transversus Abdominis Plane BlockSacral Multifidus Plane BlockLaparoscopic Colorectal Surgery
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 90
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
50 (estimated)
Sponsor
Cairo University · Other
Who this trial is looking for
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The aim of this study is to compare perioperative analgesic efficacy and safety profile of combined SMPB and posterior TAP block versus posterior TAP block in patients undergoing laparoscopic colorectal cancer surgery.
Trial Locations
Loading…
Loading trial locations…
Facility
City
State
Country
Status
Eligibility Criteria
Inclusion Criteria:
* Age between 18 and 90 years
* Male or female
* ASA class I to III
* Elective laparoscopic or robotic colorectal surgery with or without resections requiring perineal incisions.
Exclusion Criteria:
* Patient refusal
* History of previous abdominal surgery, preoperative bowel …
Inclusion Criteria:
* Age between 18 and 90 years
* Male or female
* ASA class I to III
* Elective laparoscopic or robotic colorectal surgery with or without resections requiring perineal incisions.
Exclusion Criteria:
* Patient refusal
* History of previous abdominal surgery, preoperative bowel obstruction symptoms, and requirement for emergency surgery
* Conversion to open laparotomy
* Coagulopathy, infection at the injection site, allergy to local anesthetics, body mass index \> 30 kg/m2, severe hepatic or renal disease, severe cardiopulmonary disease (≥ ASA IV), diabetic or other neuropathies, patients receiving opioids for chronic analgesic therapy, inability to comprehend visual analogue scale (VAS) and patients transferred to the intensive care unit (ICU) post-surgery.
Contacts
No contact information available.
What are you hoping to find?
Picking one helps us show the most relevant trials first.
Your results are loading in the background — you can
change this any time from the results page.
Set your location to continue
Find My Trials uses your location to surface clinical trials near you.
Add your city or zip code to your profile and try again.