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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05276440
Other study ID # KocUniversity
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 1, 2016
Est. completion date March 31, 2021

Study information

Verified date March 2022
Source Koc University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients of breast surgery dated between April 2016 and March 2021 will be scanned in three groups; solely induced general anesthesia, general anesthesia induced with Erector Spinae Plane Block, and general anesthesia induced with Rhomboid Block. The investigators aimed to retrospectively compare the effectiveness of regional anesthesia techniques used in the clinic for postoperative recovery and opioid consumption in patients who underwent breast surgery.


Recruitment information / eligibility

Status Completed
Enrollment 182
Est. completion date March 31, 2021
Est. primary completion date March 31, 2021
Accepts healthy volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Patients underwent breast surgery under general anesthesia with or without one of the blocks; Erector Spinae Plane Block and Rhomboid Block. Exclusion Criteria: - Incomplete patient forms.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Koc University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Total opioid consumption retrieved from the patient records up to 24 hours
Primary Length of hospital stay up to 1 week
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