Actively Recruiting
Effect of Adding Ultrasound Guided IPACK Block to Adductor Canal Block for Postoperative Pain in Knee Tumor Excision
Led by National Cancer Institute, Egypt · Updated on 2026-02-02
70
Participants Needed
1
Research Sites
45 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
the aim of this study is to determine the analgesic effect of iPACK in combination to ACB after the excision of tumors around the Knee regarding the following: * Time to the 1st rescue analgesia. * Postoperative morphine consumption. * Postoperative visual analogue scale (VAS). This study will include patients, aged 18 to 65 years, belonging to the American Society of Anesthesiologists (ASA) physical status II to IV , undergoing excision of tumors around the knee under spinal anesthesia. Patients will be randomly allocated Group iPACK plus Adductor canal block (ACB) : patients will receive ACB plus iPACK block. • Control group : patients will not receive any block but will take morphine 3mg bolus at VAS more than 4 and regular NSAIDS and paracetamol iv.
CONDITIONS
Official Title
Effect of Adding Ultrasound Guided IPACK Block to Adductor Canal Block for Postoperative Pain in Knee Tumor Excision
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Willingness to follow all study procedures and be available for the entire study period
- American Society of Anesthesiologists (ASA) physical status II to IV
- Scheduled for excision of tumors around the knee under spinal anesthesia
- Aged between 18 and 65 years
You will not qualify if you...
- Patient refusal to participate
- Presence of neuromuscular disorders
- Allergy to local anesthetics
- History of previous knee surgery
- History of prior knee infection
- Contraindications to spinal anesthesia such as coagulopathies or severe aortic stenosis
AI-Screening
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Trial Site Locations
Total: 1 location
1
National cancer institute
Cairo, Egypt, 11769
Actively Recruiting
Research Team
N
Norma Osama Abdallah Zayed, MD
CONTACT
F
Fady Attef, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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