ERECTOR SPINAE BLOCK AFTER THORACIC SPINE SURGERY (SPINE)

June 26, 2020 updated by: Dr Manar Mamdouh Fahmy Elsharkawi, Dubai Health Authority

THE EFFECTIVENESS OF AN ULTRASOUND GUIDED RECTOR SPINAE BLOCK IN PATIENTS UNDERGOING THORACIC SPINE SURGERY

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

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed 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

Study Type

Observational

Enrollment (Actual)

20

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

patients underging thoracic spine sugery

Description

Inclusion Criteria:

  • postoperative thoracic spine sugery

Exclusion Criteria:

  • less then 18 years
  • more than 65 years

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Randomized and Single-Arm Trials
a sham comparator (no 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
ultrasound guided erector spinae plane block can be used for postoperative analgesia for patients undergoing thoracic spine sugery
Time Frame: 2 days
postoperative analgesia
2 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Dubai Health Authority

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 26, 2018

Primary Completion (Actual)

April 22, 2020

Study Completion (Actual)

June 22, 2020

Study Registration Dates

First Submitted

June 24, 2020

First Submitted That Met QC Criteria

June 24, 2020

First Posted (Actual)

June 26, 2020

Study Record Updates

Last Update Posted (Actual)

June 30, 2020

Last Update Submitted That Met QC Criteria

June 26, 2020

Last Verified

June 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • DSREC-04/2018_01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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