Istituto Ortopedico Rizzoli
Bologna, 40136, Italy
NCT Number: NCT03075488
The study is aimed at evaluating whether ultrasound pre-procedural scan with Accuro may reduce needle redirections when performing spinal injection in patients with BMI = or > 30 in orthopedic surgery
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Notify Me18 year–75 year
All sexes
Interventional
Not applicable
Bologna, 40136, Italy
This is a open-label randomised controlled study.
90 patients will be recruited and divided into two groups of 45 patients per group.
Patient recruitment will be performed by patient visit and checking inclusions and exclusion criteria. After written informed consent, every single patient will be allocated in one of the two groups following a computer generated randomization list.
Patients in both groups will undergo:
In both groups an observer will monitor and register spinal procedure duration (starting point: anesthesiologist wearing sterile gloves, ending point: end of local anesthetic injection).
Control group (landmark technique):
The anesthesiologist will identify lumbar spinous processes with traditional landmark palpation. Once the correct interspinous level and the mid-line will be identified, the anesthesiologist will proceed with needle insertion and spinal injection.
Treatment group (ultrasound pre-procedural scan with Accuro):
By using Accuro US probe the anesthesiologist will perform a pre-procedural lumbar spine scan to detect the needle entry site. After image optimization, the Accuro probe will be aligned with the spine mid-line, as indicated by a dashed red-line on the screen. After that the interlaminar space at the desired intervertebral level will be detected, as indicated by orange overlay in the screen. The depth and the device angle used to detect the interlaminar space will be annotated. The anesthesiologist will then disengage the Accuro Locator needle guide and press gently against the skin. Then the probe will be removed and the spinal injection will be performed.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
spinal anesthesia injection based on identification of entry site with pre-procedural ultrasound scan with Accuro device
spinal anesthesia injection based on identification of entry site with palpation of cutaneous landmarks
Time frame: duration of spinal injection procedure
To evaluate if there is a significant difference about numbers of needle redirections between conventional landmark guided technique and Accuro device guided technique
Time frame: duration of spinal injection procedure
Number of needle insertions through the skin
Time frame: duration of spinal injection procedure
Procedure duration from steril gloves wearing to the end of the spinal anesthetic injection
Time frame: 36 months
To check if present side effects and complications during the procedure
Time frame: duration of surgical procedure
To check eventually procedure failure and the need of using alternative anesthesia technique
Time frame: 24 hours
Evaluation of patient satisfaction and procedure-related pain 24 hours after spinal injection
Istituto Ortopedico Rizzoli
Other
Ultrasound Pre-procedural Scan vs Conventional Landmark-guided Technique in Spinal Anesthesia in Orthopedic Obese Patients
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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