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NCT01699373 Clinical Trial

A Trial on Ultrasound-assisted Spinal Anaesthesia

Ultrasound Clinical Trial

Official title:
A Randomised Controlled Trial on Ultrasound-assisted Spinal Anaesthesia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01699373
Other study ID # UGSA/2010
Secondary ID
Status Completed
Phase N/A
First received September 30, 2012
Last updated February 27, 2013
Start date April 2011
Est. completion date May 2012

Study information
Verified date February 2013
Source Changi General Hospital
Contact n/a
Is FDA regulated No
Health authority Singapore: Institutional Review Board
Study type Interventional

Clinical Trial Summary

A randomised controlled trial comparing the use of pre-procedural ultrasound scanning with manual palpation to identify landmarks for performance of spinal anaesthesia.

Recruitment information / eligibility
Status Completed
Enrollment 170
Est. completion date May 2012
Est. primary completion date April 2012
Accepts healthy volunteers No
Gender Both
Age group 21 Years to 80 Years
Eligibility Inclusion Criteria:

- ASA I to III

- undergoing surgery amenable to spinal anaesthesia

Exclusion Criteria:

- Patient refusal

- contraindications to regional anaesthesia

- known allergy to local anaesthetics

- bleeding diathesis

- inability to provide informed consent

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• Ultrasound scan
Pre-procedural ultrasound scan was performed

Locations
Country Name City State
Singapore Changi General Hospital Singapore

Sponsors (1)
Lead Sponsor Collaborator
Changi General Hospital

Country where clinical trial is conducted

Singapore, 

Outcome
Type Measure Description Time frame Safety issue
Primary Success Rate of First-attempt of Spinal Anaesthesia During procedure No
Secondary Time Taken to Perform Spinal Anaesthesia During procedure No
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