Effect of Quadratus Lumborum Block in C/S

Sponsor

Bursa Yüksek İhtisas Education and Research Hospital (Other)

Overall Status

Completed

CT.gov ID

NCT04733313

Collaborator

(none)

143

Enrollment

Location

Arms

Actual Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief 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.

Condition or Disease	Intervention/Treatment	Phase
Postoperative Pain Cesarean Section Complications Block Patient Satisfaction	Procedure: ultrasound guıded quadratus lumborum block	N/A

Study Design

Study Type:

Interventional

Actual Enrollment :

143 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Intervention Model Description:

randomized controlledrandomized controlled

Masking:

Single (Participant)

Primary Purpose:

Prevention

Official Title:

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

Actual Study Start Date :

Jul 15, 2017

Actual Primary Completion Date :

May 15, 2018

Actual Study Completion Date :

Aug 15, 2018

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: quadratus lumborum-2	Procedure: ultrasound guıded 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.
Active Comparator: quadratus lumborum-3	Procedure: ultrasound guıded 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.

Arm

Intervention/Treatment

Active Comparator: quadratus lumborum-2

Procedure: ultrasound guıded 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.

Active Comparator: quadratus lumborum-3

Procedure: ultrasound guıded quadratus lumborum block

Outcome Measures

Primary Outcome Measures

Assesment of postoperative pain [during 24 hour after surgery]
measure of the visual analog scale at rest and dynamic after surgery

Secondary Outcome Measures

need of analgesic [during 24 hour after surgery]
total number of PCA demands

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 45 Years

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

Yes

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Healt Science University Bursa Training and Research Hospita	Bursa	Yildirim	Turkey	16310

Sponsors and Collaborators

Bursa Yüksek İhtisas Education and Research Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Ferit Yetik, medical doctor, Bursa Yüksek İhtisas Education and Research Hospital

ClinicalTrials.gov Identifier:

NCT04733313

Other Study ID Numbers:

2017-7/8

First Posted:

Feb 2, 2021

Last Update Posted:

Feb 2, 2021

Last Verified:

Jan 1, 2021

Individual Participant Data (IPD) Sharing Statement:

Plan to Share IPD:

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

Pain, Postoperative

Study Results

No Results Posted as of Feb 2, 2021