Clinical Trials Directory

Trials / Completed

CompletedNCT03683342

Comparison of Analgesic Duration of Popliteal Block Versus Ankle Block in Patients Undergoing Forefoot Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Centre Hospitalier Universitaire Vaudois · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Pain after forefoot surgery can be important and regional anesthesia plays a crucial role in post-operative pain control. Several techniques can be used to achieve surgical anesthesia as well as postoperative analgesia. Of those techniques the ankle block and sciatic nerve block at the popliteal fossa are the most common. The primary goal of this study is thus to compare the analgesic duration of these two types of blocks for patients undergoing forefoot surgery.

Detailed description

Patients scheduled for unilateral forefoot surgery, aged over 18 years old and ASA status I-III without any contra-indications for regional anesthesia will be enrolled. After a standard randomisation, patients will be allocated in either of two groups : ankle block or sciatic nerve block at the popliteal fossa. In both groups the patients will have a multimodal analgesic regimen followed by a patient-controlled-analgesia (PCA) of morphine. The primary endpoint is the analgesic duration, defined by the time between the end of the block procedure and the first IV request of morphine from a PCA.

Conditions

Interventions

TypeNameDescription
PROCEDUREAnkle BlockAnkle block will be performed prior to surgery under ultrasound guidance
PROCEDURESciatic nerve blockSciatic nerve block will be performed prior to surgery under ultrasound guidance

Timeline

Start date
2018-09-20
Primary completion
2022-11-01
Completion
2022-12-30
First posted
2018-09-25
Last updated
2023-08-03

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT03683342. Inclusion in this directory is not an endorsement.