- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01586429
Ultrasound Guided Femoral Nerve Block Catheter Analgesia Compared With Epidural Analgesia for Patients With Knee OA (Osteoarthritis) Who Underwent Unilateral Total Knee Replacement
April 25, 2012 updated by: Dr. Tariq Alzahrani, King Saud University
Post-operative pain following total knee replacement can be disabling and sometimes lead to the need for prolonged hospital stay.
Therefore development of improved post-operative modalities for total knee replacement surgery pain control is important.
High-resolution ultrasound (US) allows accurate visualization of nerves and surrounding structures and can lead to higher success rates of nerve block.
The investigators aim at comparing the analgesic efficacy of ultrasound-guided nerve block catheter compared with epidural analgesia for patients with knee OA who underwent unilateral total knee replacement.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
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: Tariq A Alzahrani, MD
- Phone Number: +966555702334
- Email: talzahrani@ksu.edu.sa
Study Locations
-
-
-
Riyadh Region, Saudi Arabia
- Recruiting
- King Saud University
-
Contact:
- Tariq A Alzahrani, MD
- Phone Number: +966555702334
- Email: talzahrani@ksu.edu.sa
-
Principal Investigator:
- Tariq A Alzahrani, MD
-
-
Riyadh Region
-
Riyadh, Riyadh Region, Saudi Arabia
- Recruiting
- King Saud University
-
Contact:
- Tariq A Alzahrani, MD
- Phone Number: +966555702334
- Email: talzahrani@ksu.edu.sa
-
Principal Investigator:
- Tariq A Alzahrani, MD
-
-
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
30 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
for patients with knee OA (osteoarthritis) who underwent unilateral total knee replacement.
Description
Inclusion Criteria:
- Male / female, Bilateral or unilateral knee OA (Osteoarthritis), and ASA (American Society of Anesthesiologist classification) 1 and 2.
Exclusion Criteria:
- Bilateral total knee replacement, Revision total knee replacement, previous knee surgery, Rheumatoid Arthritis, Avascular necrosis (AVN) knee, Post traumatic or post infectious OA, ASA3 and 4.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Epidural
|
|
Femoral catheter
|
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 Registration Dates
First Submitted
April 25, 2012
First Submitted That Met QC Criteria
April 25, 2012
First Posted (Estimate)
April 26, 2012
Study Record Updates
Last Update Posted (Estimate)
April 26, 2012
Last Update Submitted That Met QC Criteria
April 25, 2012
Last Verified
February 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E-12-589
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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