CClinicalTrials.gg
Status unknownNCT01322126Updated Apr 11, 2011

Comparison of Safety And Efficacy of Neuraxial Anesthesia, Palpation Versus Ultrasound

An interventional study of ultrasound probe in Regional Anesthesia, sponsored by Hadassah Medical Organization. Status unknown at 1 site in Israel. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2011-04-11.

Sponsored by Hadassah Medical Organization · Not applicable, Interventional, and Supportive care

The sponsor has not verified this record recently (last verified Mar 2011), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to determine whether use of the ultrasound to locate the epidural space and assist with performing neuraxial anesthesia will decrease numbers of the attempts required for successful placement of epidural catheter.

Read the detailed description

It is known that ultrasound can be useful to assist placement of epidural analgesia among pregnant women.extenseve research on the usefulness of ultrasound imaging to facilitate the placement of neuraxial anesthesia in pregnant have been done.The potential advantages of successful placement among non-pregnant patients include increases the safety and comfort.

In our study all patients schedueld to receive an nueraxial anesthesia for non-obstetric surgery will be included.The investigator will request permission from the Helsinki committee of hadassah university hospital.Patients will be requesting for surgery and will be randomized to one of two study groups.One group will be passed neuraxial anesthesia on the standart technique and the secound group will be passed neuraxial anesthesia with the help of ultrasound.

02

Conditions studied

  • Regional Anesthesia
03

In context

Lead sponsor

Hadassah Medical Organization is the lead sponsor of 659 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • all patients scheduled for neuraxial anesthesia

Exclusion criteria

Exclusion Criteria:

  • previous spine surgery
  • contraindication for neuraxial anesthesia
  • refusing to sign the consent form
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    ultrasound ,without ultrasound

    ultrasound group will be passed the neuraxial anesthesia with ultrasound,the secoud group will be passed the neuraxial anesthesia without ultrasound .

    Device: ultrasound probe

Interventions

  • Deviceultrasound probe

    we will compare two technique of neuraxial anesthesia;one group will be passed neuraxial anesthesia with the intervention the ultrasound and the other group without the intervention of the ultrasound.

06

What researchers measure

Primary outcomes

  1. Number of epidural attempts made to succeed for placing epidural needle and catheter in epidural space

    Each attempt at placing epidural needle in epidural space will be recorded. Total number of attempts will be recorded

    Time frame: one year

Secondary outcomes

  1. patient satisfaction as measured by VAS (0=not satisfied, 10 = most satisfied)

    Time frame: one year

07

Study locations

1 site
  • Hadassah Medical Organization
    Jerusalem 91120, P.O.BOX 12000, Israel
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 11, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01322126
Lead sponsor
Hadassah Medical Organization
First posted
Mar 24, 2011
Start date
Apr 2011
Primary completion
Apr 2012 (estimated)
Completion
Apr 2012 (estimated)
Last update
Apr 11, 2011

Study contacts

Fayez T Saifi, MD
Contact
saififayez@gmail.com
00972508946127
Hadas Lemberg, PhD
Contact
lhadas@hadassah.org.il
0097226777572
Fayez T Saifi, MD
principal investigator · Hadassah Medical Organization

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2011. You cannot join it, but the record below documents what was studied.

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