ERECTOR SPINAE BLOCK AFTER THORACIC SPINE SURGERY

Sponsor
Dubai Health Authority (Other)
Overall Status
Completed
CT.gov ID
NCT04449367
Collaborator
(none)
20
1
21.9
0.9

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Procedure: ultrasound guided erector spinae plane block

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 Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
20 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
THE EFFECTIVENESS OF AN ULTRASOUND GUIDED RECTOR SPINAE BLOCK IN PATIENTS UNDERGOING THORACIC SPINE SURGERY
Actual Study Start Date :
Aug 26, 2018
Actual Primary Completion Date :
Apr 22, 2020
Actual Study Completion Date :
Jun 22, 2020

Arms and Interventions

Arm 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

Outcome Measures

Primary Outcome Measures

  1. ultrasound guided erector spinae plane block can be used for postoperative analgesia for patients undergoing thoracic spine sugery [2 days]

    postoperative analgesia

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • postoperative thoracic spine sugery
Exclusion Criteria:
  • less then 18 years

  • more than 65 years

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dubai Health Authority Dubai United Arab Emirates

Sponsors and Collaborators

  • Dubai Health Authority

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr Manar Mamdouh Fahmy Elsharkawi, SPECIALIST ANAESTHESIOLOGIST, Dubai Health Authority
ClinicalTrials.gov Identifier:
NCT04449367
Other Study ID Numbers:
  • DSREC-04/2018_01
First Posted:
Jun 26, 2020
Last Update Posted:
Jun 30, 2020
Last Verified:
Jun 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jun 30, 2020