Actively Recruiting
Analgesic Effects of Fentanyl Versus Dexmedetomidine with Bupivacaine in Combined IPACK and Adductor Canal Block for Pain Relief After Knee Surgery
Led by Zagazig University · Updated on 2025-01-14
111
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the pain relief effects of fentanyl versus dexmedetomidine when added to bupivacaine in combined IPACK and Adductor Canal Block (ACB) techniques after knee surgeries. The goal is to compare these two drugs as additional agents to manage postoperative pain following total knee arthroplasty and other knee procedures. The study includes adults aged 21 to 85 undergoing elective unilateral knee surgeries such as total knee arthroplasty, ACL reconstruction, or knee arthroscopy. Participants are divided into three groups. One group receives bupivacaine alone in the blocks, the second group receives bupivacaine plus fentanyl, and the third group receives bupivacaine plus dexmedetomidine. Each block is given via ultrasound guidance with 20 mL of 0.25% bupivacaine plus either saline, 50 mcg fentanyl, or up to 100 mcg dexmedetomidine. Treatments are applied to the knee area using the combined IPACK and ACB techniques. During the 48 hours after surgery, patients' pain levels at rest and during knee movement are assessed at several time points using a numerical rating scale. The total amount of rescue pain medication (tramadol) used is recorded, along with the time to first rescue analgesia. Researchers also monitor side effects such as hematoma, local anesthetic toxicity, infection, nausea, vomiting, and length of hospital stay. Patients will rate their overall satisfaction with pain relief using a five-point scale.
CONDITIONS
Official Title
Comparison Between Fentanyl and Dexmedetomidine As Adjuvant to Bupivacaine in Combined IPACK and Adductor Canal Block for Postoperative Analgesia After Knee Surgeries
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient acceptance
- Cooperative patients
- Age between 21 and 85 years old
- Both males and females
- Physical status ASA I, II, or III
- Body Mass Index (BMI) of 35 kg/m2 or less
- Undergoing elective unilateral knee surgeries (total knee arthroplasty, ACL reconstruction, or knee arthroscopy)
You will not qualify if you...
- Any contraindications to regional blocks such as coagulopathy or local infection at the injection site
- Known allergy to bupivacaine, dexmedetomidine, or fentanyl
- Advanced liver, kidney, heart, neurological, or respiratory diseases
- Chronic opioid use exceeding 3 months or daily oral morphine use above 5 mg for 1 month
AI-Screening
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Trial Site Locations
Total: 1 location
1
faculty of human medicine, Zagazig university hospitals
El Sharkia, Egypt
Actively Recruiting
Research Team
D
Dina Sadek Salem, MD
S
Sherif Mowafy, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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