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NCT03853460 Clinical Trial

Bilateral Quadraus LUMBORUM Block in Patients Under Going Cystectomy

Pain, Acute Clinical Trial

Official title:
Bilateral Quadraus LUMBORUM Block in Patients Under Going Cystectomy

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03853460
Other study ID # QLMD
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 30, 2019
Est. completion date December 30, 2020

Study information
Verified date November 2019
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

ultrasound guided quadratus lumborum will be given for patients under going partial or complete urinary bladder removal.

Description:

ultrasound guided quadratus lumborum will be given for patients under going partial or complete urinary bladder removal.

Recruitment information / eligibility
Status Recruiting
Enrollment 60
Est. completion date December 30, 2020
Est. primary completion date May 30, 2020
Accepts healthy volunteers No
Gender All
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria:

- elective surgery

- patients between 30 and 60 years

Exclusion Criteria:

- coagulopathy

- infection at insertion site

- patient refusal

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• epidural catheter
ultrasound low frequency probe will be used to determine the depth of the posterior complex to assists placement of midline thoracic epidural
• nerve block catheter
ultrasound guided placement of bilateral quadratus lumborum catheters

Locations
Country Name City State
Egypt Assiut university Assiut
Egypt Faculty of Medicine Asyut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain score Visual analogue score from 0 to 10 will be used to assess pain postoperative. 0 means no pain. 10 is worst pain 24 hours
Secondary anaesthetic consumption calculating the total anaesthetic MAC consumed 4 hours
Secondary diaphragmatic excursion assessment of diaphragmatic excursion preoperative and postoperative using low frequency ultrasound probe 24 hours
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