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NCT04733313 Clinical Trial

Effect of Quadratus Lumborum Block in C/S

Postoperative Pain Clinical Trial

Official title:
Comparison of Ultrasound Guided Quadratus Lumborum Block-2 and Quadratus Lumborum Block-3 for Postoperative Pain in Cesarean Section

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04733313
Other study ID # 2017-7/8
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 15, 2017
Est. completion date August 15, 2018

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

Clinical Trial Summary

to compare postoperative analgesic effects of USG guided QLB-2 and QLB-3 blocks after C/S. We hypothesized that QLB-3 may be more effective for pain relieving than QLB-2 after C/S.

Recruitment information / eligibility
Status Completed
Enrollment 143
Est. completion date August 15, 2018
Est. primary completion date May 15, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - pregnancy with a gestation of 37-41 weeks parturients who were scheduled for elective cesarean delivery under general anesthesia - obtained patients informed consent Exclusion Criteria: - inability to comprehend - bleeding diathesis - allergy to the study agents - localized infection - block failure

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• ultrasound guided quadratus lumborum block
Administering local aneshtetic agent with a block needle using the in-plane technique, bilaterally. Lumbar interfascial triangle, where the middle lumbar fascia joins the deep lamina of the posterior layer on the lateral border of the erector spinae was targeted as the optimal point of injection.

Locations
Country Name City State
Turkey Healt Science University Bursa Training and Research Hospita Bursa Yildirim

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 Assesment of postoperative pain measure of the visual analog scale at rest and dynamic after surgery during 24 hour after surgery
Secondary need of analgesic total number of PCA demands during 24 hour after surgery
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