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NCT05473559 Clinical Trial

Comparison Between the Effect of Infiltration Between the Popliteal Artery and Capsule of the Knee Block Versus Selective Tibial Nerve Block for Postoperative Analgesia in Patient Undergoing Total Knee Arthroplasty. A Prospective Randomized Study

Postoperative Analgesia Clinical Trial

Official title:
Comparison Between i Pack Block and Post Tibial Nerve Block

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05473559
Other study ID # 35151/12/21
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date June 30, 2022

Study information
Verified date December 2021
Source Tanta University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison Between the Effect of Infiltration Between the Popliteal Artery and Capsule of the Knee Block Versus Selective Tibial Nerve Block for Postoperative Analgesia in Patient Undergoing Total Knee Arthroplasty.

Recruitment information / eligibility
Status Completed
Enrollment 70
Est. completion date June 30, 2022
Est. primary completion date June 15, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria: - Patients with osteoarthritis scheduled for a primary either partial or total knee arthroplasty • Patients aged 40-80 years with a body mass index of 18-36 kg/ m2 and an American Society of Anesthesiologists functional status of I-III Planned use of regional anesthesia Exclusion Criteria: - • Patients younger than 40 years old and older than 80years. - Hepatic or renal insufficiency. - Patients undergoing general anesthesia. - Allergy or intolerance to one of the study medications. - BMI > 36 - Diabetes - ASA of IV - Chronic opioid use (taking opioids for longer than 3 months, or daily oral morphine equivalent of >5mg/day for one month)

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Adductor canal block with Ipack block or selective tibial nerve block
Ultrasound guided

Locations
Country Name City State
Egypt Tanta university Tanta

Sponsors (1)
Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Total morphine consumption 24 hours 24 hours post operative
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