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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04370951
Other study ID # 1/378/2088
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 1, 2020
Est. completion date January 3, 2021

Study information

Verified date May 2020
Source Mater Misericordiae University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Spinal Surgery can be associated with significant post operative pain. This can be a considerable source of morbidity, resulting in a longer duration of in- hospital stay and increasing opiate requirements. As a result the patient experiences a more arduous recovery process.

Recently a new form of Regional Anaesthesia has been described for patients undergoing Spinal surgery. The Erector Spinae Plane Block involves depositing Local Anaesthetic under Ultra Sound guidance on top of the Transverse Process of the Spine and deep to the Erector Spinae Muscle. Patients who have had this procedure report lower pain scores and have a lesser opiate requirement in the post operative period.


Description:

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Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Erector Spinae Plane Block - Ultrasound guided
20mls 0.25% Levobupivicaine ultrasound guided bilaterally

Locations

Country Name City State
Ireland Mater Misericordiae University Hospital Dublin

Sponsors (1)

Lead Sponsor Collaborator
Mater Misericordiae University Hospital

Country where clinical trial is conducted

Ireland, 

Outcome

Type Measure Description Time frame Safety issue
Primary QoR 15 score a objective assessment of quality of recovery post surgery 24 hours post operatively
Secondary AUC of VRS Pain score versus time Area under the VRS pain score versus time 24 hours post op
Secondary time to administration of first rescue analgesia after the block 24 hours post op
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