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NCT04738500 Clinical Trial

Postoperative Analgesic Efficacy of Pericapsular Nerve Group Block (PENG) Block for Knee Arthroscopy

Postoperative Pain Clinical Trial

Official title:
Postoperative Analgesic Efficacy of Pericapsular Nerve Group Block (PENG) Block for Knee Arthroscopy

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04738500
Other study ID # 123
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 15, 2021
Est. completion date June 15, 2021

Study information
Verified date April 2021
Source Kahramanmaras Sutcu Imam University
Contact Bora Bilal, Assos. Prof.
Phone 05052354430
Email bilalbora@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pericapsular nerve group block (PENG) has been deemed as a safe and effective regional technique for postoperative pain after knee arthroscopy.

Description:

Pericapsular nerve group block(PENG) has been deemed as a safe and effective regional technique for postoperative pain after knee artroscopy. Blockade of the branches of the femoral and obturator nerves that provide innervation to any structures distal enough to be useful in knee.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 60
Est. completion date June 15, 2021
Est. primary completion date May 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Patients agreed to receive PENG block - Knee arthroscopy Exclusion Criteria: - Other kinds of knee surgery - Patients refuse to receive PENG block

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• PENG Block combinated with PCA
After spinal anesthesia PENG block will be performed
• PCA
PCA will be applied after surgery

Locations
Country Name City State
Turkey KSU Faculty of Medicine Research Hospital Kahramanmaras

Sponsors (1)
Lead Sponsor Collaborator
Bora Bilal

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary First analgesic demand The time interval from PENG blocks to the first analgesic demand. 24 Hours
Secondary Opioid consumption Total opioid analgesic consumption 24 Hours
Secondary Numeric Rating Scale The maximum score on a 10cm numeric rating scale: (0 to 10cm) (0 = no pain, 10 = worst imaginable pain) 24 Hours
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