Clinical Trials Directory

Trials / Completed

CompletedNCT06489210

A Comparison Between Posterior, Lateral and Medial Approaches for Ultrasound-guided Popliteal Block

A Comparison Between Posterior, Lateral and Medial Approaches for Ultrasound-guided Popliteal Block: A Randomized Clinical Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Helwan University · Academic / Other
Sex
All
Age
21 Years – 50 Years
Healthy volunteers
Accepted

Summary

Background: Popliteal block is a widely used technique to provide anesthesia or analgesia for below-knee surgical procedures. In this study, the investigators compare ultrasound-guided popliteal blocks via posterior, lateral, and medial approaches to find out the approach with the best outcome.

Detailed description

Methods: In this randomized, controlled clinical trial, one hundred and twenty ASA physical status of class I and II patients undergoing below-knee surgery were involved. These patients were divided into three equal groups at randomly based on the route assigned for the US-guided popliteal block: the posterior, lateral, and medial approach groups. In this study, technical characteristics \[number of attempts to get the proper injection site and block performance time\], anesthetic and analgesic characteristics \[success rate, block onset, potency, and duration, time to ask, and the consumed amount of postoperative analgesia\], discomfort rate in respect to position and needle insertion and the associated complications were recorded.

Conditions

Interventions

TypeNameDescription
PROCEDUREpopliteal blockusing ultrasound to detect sciatic nerve and popliteal fossa through different approaches using 20ml of the selected local anesthetic mixture (10ml of 0.5% bupivacaine mixed with 10ml of 2% lidocaine, each with 1:200,000 epinephrine) was injected incrementally

Timeline

Start date
2018-04-01
Primary completion
2021-04-30
Completion
2021-04-30
First posted
2024-07-05
Last updated
2024-07-05

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06489210. Inclusion in this directory is not an endorsement.