ERECTOR SPINAE BLOCK AFTER THORACIC SPINE SURGERY

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

Completed

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Key information

Conditions

Post Operative Analgesia

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Dubai Health Authority

Dubai, United Arab Emirates

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

postoperative thoracic spine sugery

Exclusion criteria

less then 18 years
more than 65 years

Treatment and study plan

Ultrasound guided Erector Spinae Plane block

Procedure

bilatral block given to patients under general anaesthesia for thoracic spine sugery to contorl post operative pain

Primary outcomes

ultrasound guided erector spinae plane block can be used for postoperative analgesia for patients undergoing thoracic spine sugery

Time frame: 2 days

postoperative analgesia

Sponsors and collaborators

Lead sponsor

Dubai Health Authority

Other Gov

Registry information

Official study title

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

Acronym: SPINE

Important dates

Study start: 2018
Primary completion: 2020
Study completion: 2020
First posted: Jun 26, 2020
Registry last updated: Jun 30, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed