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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04449367
Other study ID # DSREC-04/2018_01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 26, 2018
Est. completion date June 22, 2020

Study information

Verified date June 2020
Source Dubai Health Authority
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

the effectiveness of ultrasound guided erector spinae plane block in patients undergoing thoracic spine sugery


Description:

bilateral erector spinae plane block would be given to patients with thoracic spine sugery for postoperative analgesia & its effectiveness would be evaluated for 2 days


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 22, 2020
Est. primary completion date April 22, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- postoperative thoracic spine sugery

Exclusion Criteria:

- less then 18 years

- more than 65 years

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ultrasound guided erector spinae plane block
bilatral block given to patients under general anaesthesia for thoracic spine sugery to contorl post operative pain

Locations

Country Name City State
United Arab Emirates Dubai Health Authority Dubai

Sponsors (1)

Lead Sponsor Collaborator
Dubai Health Authority

Country where clinical trial is conducted

United Arab Emirates, 

Outcome

Type Measure Description Time frame Safety issue
Primary ultrasound guided erector spinae plane block can be used for postoperative analgesia for patients undergoing thoracic spine sugery postoperative analgesia 2 days
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