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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04805580
Other study ID # Qudratus lumborum block
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 2021
Est. completion date October 2021

Study information

Verified date April 2021
Source Zagazig University
Contact Hala Rashad
Phone +201148737769
Email rashad_hala@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

compare between Quadratus lumborum block and unilateral intrathecal block for patients undergoing inguinal hernia repair regarding the quality of anesthesia and hemodynamic stability of patients.


Description:

comparison between unilateral intrathecal block anesthesia (unilateral SA) and Quadratus lumborum block for inguinal hernia repair unilateral intrathecal block is widely used nowadays for unilateral inguinal hernia repair, providing intense sensory and motor blockade. Limiting the block to the operative site by using small doses of hyperbaric solutions injected slowly through a directional needle and maintaining a lateral decubitus position for a certain duration has been proposed, to produce high quality, long-duration analgesia, with minimal hemodynamic adverse events. Previous case report studies stated that we can use Quadratus Lumborum Block as the sole anesthetic technique for open hernia repair.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date October 2021
Est. primary completion date September 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - physical status ASA: I-II BMI >18kg/m2<30kg/m2 written informed consent from the patient scheduled for open unilateral inguinal hernia repair Exclusion Criteria: - uncooperative patient - Allergy to local anesthetic drugs - patients on chronic alcohol, opioid, tranquilizer or sedative use - Pregnant females. - Psychological, mental disorders, or depression. - Patients receiving anticoagulants therapy or suspected coagulopathy. - Patients with infection or previous surgery at sit of anesthetic procedures. - Patients with significant cardiovascular, respiratory, renal, hepatic, or metabolic disease

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
unilateral intrathecal block
Quadratus lunborum block

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Zagazig University

References & Publications (3)

Favaro ML, Gabor S, Souza DBF, Araújo AA, Milani ALC, Ribeiro Junior MAF. Quadratus Lumborum Block As A Single Anesthetic Method For Laparoscopic Totally Extraperitoneal (Tep) Inguinal Hernia Repair: A Randomized Clinical Trial. Sci Rep. 2020 May 22;10(1):8526. doi: 10.1038/s41598-020-65604-x. — View Citation

Isil CT, Çinar AS, Oba S, Isil RG. Comparison of Spinal Anaesthesia and Paravertebral Block in Unilateral Inguinal Hernia Repair. Turk J Anaesthesiol Reanim. 2014 Oct;42(5):257-63. doi: 10.5152/TJAR.2014.75508. Epub 2014 Jul 9. — View Citation

La Colla L, La Colla MDL, Schroeder R, Schroeder RMD. Quadratus Lumborum Block as Sole, Homeostatic-Preserving Anesthetic for a Patient with Multiple System Atrophy Undergoing Open Inguinal Hernia Repair: A Case Report. Case Rep Anesthesiol. 2018 Jun 28;2018:7161860. doi: 10.1155/2018/7161860. eCollection 2018. Erratum in: Case Rep Anesthesiol. 2018 Aug 19;2018:8316750. La Colla MDL [corrected to La Colla L], Schroeder RMD [corrected to Schroeder R]. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary To assess safety of quadratus lumborum block vs unilateral intrathecal block for inguinal hernia repair: complications of the block complications of the block in each group like inadequate blockade detected by increased dose of sedation required in this group ,hemodynamic instability related to the block detected by frequent monitoring of the blood pressure and heart rate 2 hours
Secondary To compare the onset and duration of sensory block between both blocks the onset of pin brick discrimination and time of first request of analgesics after block performance in each group 12 hours
Secondary To compare the time to ambulation the time till the patient succeed in ambulation 24 hours