Bilateral Quadraus LUMBORUM Block in Patients Under Going Cystectomy

NCT ID: NCT03853460

Last Updated: 2019-11-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-10-30

Study Completion Date

2020-12-30

Brief Summary

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

Detailed Description

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

Conditions

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Pain, Acute

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Outcome Assessors
both patients and data collector will be unaware of the group nature

Study Groups

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epidural group

ULTRASOUND GUIDED thoracic epidural at T 12 WILL BE INSERTED before anaesthesia induction

Group Type ACTIVE_COMPARATOR

epidural catheter

Intervention Type PROCEDURE

ultrasound low frequency probe will be used to determine the depth of the posterior complex to assists placement of midline thoracic epidural

quadus lumborum group

bilateral ultrasound guided quadratus lumborum catheter will be inserted before anaesthesia induction

Group Type ACTIVE_COMPARATOR

nerve block catheter

Intervention Type PROCEDURE

ultrasound guided placement of bilateral quadratus lumborum catheters

Interventions

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epidural catheter

ultrasound low frequency probe will be used to determine the depth of the posterior complex to assists placement of midline thoracic epidural

Intervention Type PROCEDURE

nerve block catheter

ultrasound guided placement of bilateral quadratus lumborum catheters

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* elective surgery
* patients between 30 and 60 years

Exclusion Criteria

* coagulopathy
* infection at insertion site
* patient refusal
Minimum Eligible Age

30 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Rasha Hamed

lecturer of anaesthesia and pain management

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Assiut university

Asyut, , Egypt

Site Status RECRUITING

Faculty of Medicine

Asyut, , Egypt

Site Status RECRUITING

Countries

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Egypt

Facility Contacts

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rasha hamed, MD

Role: primary

0882413201

rasha hamed

Role: primary

01000440773

saeed elsawy

Role: backup

01030072161

Other Identifiers

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QLMD

Identifier Type: -

Identifier Source: org_study_id

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