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NCT03679663

Ultrasound Versus Palpation for Spinal Anesthesia Success

Prospective Randomized Controlled Trial to Compare a Handheld Ultrasound Identification of the Neuraxial Block Insertion Site Versus Palpation Only in an Obese Population of Women Undergoing Cesarean Delivery
Tel-Aviv Sourasky Medical Center·ClinicalTrials.gov·device·Device trialCompleted
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Study focus
Disease/Condition
Ultrasound
Drug/Device/Intervention
Ultrasound
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
Tel-Aviv Sourasky Medical Center
Location
Tel Aviv, Israel
Timeline & enrollment
Phase
N/A
Start date
Dec 20, 2018
End date
Aug 04, 2020
Enrollment
40 participants
Primary outcome

Needle movement

Summary

Aim is to investigate the difference in number of attempts to place neuraxial block comparing
 handheld ultrasound versus use of palpation alone for women with impalpable bony landmarks
 undergoing spinal anesthesia for elective cesarean delivery.

ICD-10 classifications
Abnormal ultrasonic finding on antenatal screening of motherAntenatal screening for malformations using ultrasound and other physical methodsAntenatal screening for fetal growth retardation using ultrasound and other physical methodsOther diagnostic agentsExamination of ears and hearing
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT03679663
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT03679663 through Pure Global AI's free database. This phase not specified trial is sponsored by Tel-Aviv Sourasky Medical Center and is currently Completed. The study focuses on Ultrasound. Target enrollment is 40 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.