Status:
RECRUITING
Multimodal Analgesia vs. Femoral Block in ACL Surgery
Lead Sponsor:
Ankara University
Conditions:
Anterior Cruciate Ligament Injuries
Postoperative Pain
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
This study aims to compare the effects of a preemptive multimodal intravenous analgesia protocol and a femoral triangle block on early postoperative rehabilitation compliance in patients undergoing an...
Detailed Description
Postoperative pain following anterior cruciate ligament (ACL) reconstruction is typically acute in nature and may hinder early physiotherapy interventions. Effective postoperative pain control is esse...
Eligibility Criteria
Inclusion
- Age: 18 years or older. Condition: Patients scheduled for anterior cruciate ligament (ACL) reconstruction surgery.
- ASA Classification: Patients classified as ASA I, II, or III. Orientation: Patients who are fully oriented and can cooperate with study procedures.
- Consent: Patients capable of providing informed consent to participate in the study.
Exclusion
- Informed Consent: Patients unable to provide informed consent. BMI: Patients with a BMI of ≥30 kg/m². Allergy: Known allergy to local anesthetics. Orientation and Cooperation: Patients who are not fully oriented or cannot cooperate with study procedures.
- Additional Trauma: Patients with other traumatic injuries requiring opioid analgesia.
- Neuropathic Pain History: Patients with a history of neuropathic pain. Chronic Pain Syndrome: Patients with a history of chronic pain syndrome.
Key Trial Info
Start Date :
January 21 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 20 2026
Estimated Enrollment :
62 Patients enrolled
Trial Details
Trial ID
NCT06936995
Start Date
January 21 2025
End Date
January 20 2026
Last Update
April 20 2025
Active Locations (1)
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1
Ankara University Faculty of Medicine
Ankara, Turkey (Türkiye), 06230