Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06936995

Multimodal Analgesia vs. Femoral Block in ACL Surgery

Led by Ankara University · Updated on 2025-04-20

62

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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 anterior cruciate ligament (ACL) reconstruction under general anesthesia. Adult patients aged 18 to 65 will be randomized to receive either multimodal intravenous analgesia or femoral triangle block prior to surgery. Rehabilitation compliance will be evaluated using the straight leg raise test, sit-to-stand success, and pain scores at multiple postoperative time points. Secondary outcomes include opioid consumption, incidence of opioid-related side effects.

CONDITIONS

Official Title

Multimodal Analgesia vs. Femoral Block in ACL Surgery

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Scheduled for anterior cruciate ligament (ACL) reconstruction surgery
  • Classified as ASA physical status I, II, or III
  • Fully oriented and able to cooperate with study procedures
  • Capable of providing informed consent to participate in the study
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent
  • Body mass index (BMI) of 30 kg/m² or higher
  • Known allergy to local anesthetics
  • Not fully oriented or unable to cooperate with study procedures
  • Presence of other traumatic injuries requiring opioid analgesia
  • History of neuropathic pain
  • History of chronic pain syndrome

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ankara University Faculty of Medicine

Ankara, Turkey (Türkiye), 06230

Actively Recruiting

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Research Team

S

SEVDE NUR AYDIN KUŞSAN, Research Assistant

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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