NCT04449367

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Aug 2018

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 26, 2018

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 22, 2020

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 22, 2020

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

June 24, 2020

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 26, 2020

Completed
Last Updated

June 30, 2020

Status Verified

June 1, 2020

Enrollment Period

1.7 years

First QC Date

June 24, 2020

Last Update Submit

June 26, 2020

Conditions

Post Operative Analgesia

Outcome Measures

Primary Outcomes (1)

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

    postoperative analgesia

    2 days

Study Arms (1)

Randomized and Single-Arm Trials

a sham comparator (no intervention)

Procedure: ultrasound guided erector spinae plane block

Interventions

ultrasound guided erector spinae plane blockPROCEDURE

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

Randomized and Single-Arm Trials

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients underging thoracic spine sugery

You may qualify if:

  • postoperative thoracic spine sugery

You may not qualify if:

  • less then 18 years
  • more than 65 years

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dubai Health Authority

Dubai, United Arab Emirates

Location

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
2 Days
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
SPECIALIST ANAESTHESIOLOGIST

Study Record Dates

First Submitted

June 24, 2020

First Posted

June 26, 2020

Study Start

August 26, 2018

Primary Completion

April 22, 2020

Study Completion

June 22, 2020

Last Updated

June 30, 2020

Record last verified: 2020-06

Data Sharing

IPD Sharing
Will not share

Locations

AE(1)