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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04264689
Other study ID # AP1906-50105
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2, 2020
Est. completion date November 3, 2020

Study information

Verified date December 2020
Source National Cancer Institute, Egypt
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the study aim is to compare the analgesic effect of thoracic epidural versus serratus plane block versus erector spinae block in thoracic surgeries


Description:

comparing the analgesic effect of thoracic epidural versus serratus plane block versus erector spinae block in thoracic surgeries regarding pain control and possible side effects


Recruitment information / eligibility

Status Completed
Enrollment 51
Est. completion date November 3, 2020
Est. primary completion date October 28, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - patients scheduled for thoracotomy age 18-65 Exclusion Criteria: - patient refusal coagulation defects abnormal kidney or liver functions local infection at site of block bone metastases

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
serratus anterior block
ultrasound guided block
thoracic epidural
thoracic epidural
erector spinae block
ultrasound guided block

Locations

Country Name City State
Egypt Department of anesthesia and pain medicine. National Cancer Institute Cairo

Sponsors (1)

Lead Sponsor Collaborator
National Cancer Institute, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary visual analogue score minimum value 0 and maximum value 10 24 hours
Secondary mean arterial blood pressure measurement of mean arterial blood pressure 24 hours
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