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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04094987
Other study ID # 2011-KAEK-25 2019/05-26
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 29, 2019
Est. completion date September 15, 2020

Study information

Verified date February 2021
Source Bursa Yüksek Ihtisas Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The block has been shown to be the result of abdominal analgesia as a result of application between the quadratus lumborum (QL) muscle and the leaves in the thoracolumbar fascia. In this block, local anesthetic drugs are administered between the quadratus lumborum (QL) muscle and the anterior leaf in the thoracolumbar fascia. In this way, it has been reported that it provides a good analgesia as it relieves somatic pain better in upper and lower abdominal surgeries.


Description:

The mechanism of QLB analgesic contains many theories. This study includes the research relationship between the effect of fascial pressure and the success of the association block. We will use the ultrasound guided anterior Quadratus Lumborum Block. A peripheral nerve block catheter will be placed between the quadratus lumborum muscle and the psoas muscle with ultrasound.The pressure between the fascia and the pressure line added to the catheter tip will be measured.A peripheral nerve block catheter will be placed between the quadratus lumborum muscle and the psoas muscle with ultrasound. The pressure between the fascia and the pressure line added to the catheter tip will be measured.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date September 15, 2020
Est. primary completion date October 15, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: Patients who were in the American Society of Anesthesiologists (ASA) I-III class • Underwent laparoscopic cholecystectomy Exclusion Criteria: - Previous history of preoperative opioid use, - Allergy to local anesthetics, - The presence of any systemic infection, - Uncontrolled arterial hypertension, - Uncontrolled diabetes mellitus - Presence of infection in the block area,

Study Design


Related Conditions & MeSH terms


Intervention

Device:
inter-fascial pressure
The pressure between the fascia and the pressure line added to the catheter tip will be measured.

Locations

Country Name City State
Turkey University of Health Sciences, Bursa Yuksek Ihtisas Training and Research Hospital Bursa

Sponsors (1)

Lead Sponsor Collaborator
Bursa Yüksek Ihtisas Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Interfascial Pressure (mm/hg) Interfascial pressure will be measured the postoperative 24. hours through catheter. 24 hours.
Secondary sensory block level After the application, the sensory block level at the 30 minutes after the block application and 30 minutes after the operation will be determined by cold test. peroperative 3 hours
Secondary Visual Analog Scale Visual Analog Scale was used for pain.Pain intensity was measured using 0-10 cm visual analogue scale (VAS). (0=no pain, 10=intolerable pain) Postoperative 24 hours
Secondary analgesic use analgesic use Postoperative 24 hours
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