- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04738500
Postoperative Analgesic Efficacy of Pericapsular Nerve Group Block (PENG) Block for Knee Arthroscopy
April 13, 2021 updated by: Bora Bilal
Pericapsular nerve group block (PENG) has been deemed as a safe and effective regional technique for postoperative pain after knee arthroscopy.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed 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.
Study Type
Interventional
Enrollment (Anticipated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Bora Bilal, Assos. Prof.
- Phone Number: 05052354430
- Email: bilalbora@yahoo.com
Study Locations
-
-
-
Kahramanmaraş, Turkey, 46200
- KSU Faculty of Medicine Research Hospital
-
Contact:
- Bora Bilal
- Phone Number: 03443003245
- Email: bbilal@ksu.edu.tr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients agreed to receive PENG block
- Knee arthroscopy
Exclusion Criteria:
- Other kinds of knee surgery
- Patients refuse to receive PENG block
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
ACTIVE_COMPARATOR: PENG Block
PENG Block combinate with PCA
|
After spinal anesthesia PENG block will be performed
Other Names:
|
SHAM_COMPARATOR: CONTROL
PCA
|
PCA will be applied after surgery
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
First analgesic demand
Time Frame: 24 Hours
|
The time interval from PENG blocks to the first analgesic demand.
|
24 Hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Opioid consumption
Time Frame: 24 Hours
|
Total opioid analgesic consumption
|
24 Hours
|
Numeric Rating Scale
Time Frame: 24 Hours
|
The maximum score on a 10cm numeric rating scale: (0 to 10cm) (0 = no pain, 10 = worst imaginable pain)
|
24 Hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ANTICIPATED)
April 15, 2021
Primary Completion (ANTICIPATED)
May 30, 2021
Study Completion (ANTICIPATED)
June 15, 2021
Study Registration Dates
First Submitted
February 1, 2021
First Submitted That Met QC Criteria
February 1, 2021
First Posted (ACTUAL)
February 4, 2021
Study Record Updates
Last Update Posted (ACTUAL)
April 14, 2021
Last Update Submitted That Met QC Criteria
April 13, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 123 (Giresun University Scientific Research Project)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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