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Taking people in United StatesPhase 4

Testing a numbing injection near the thigh artery for tourniquet-related high blood pressure

Tests a numbing drug injected near the femoral artery in adults having ankle surgery.

Plain-language title generated from the registry record
Registry title: Femoral Peri-arterial Local Anesthetic Injection Via Peri-arterial Perineural Catheter Reverses Tourniquet Associated Ischemic Hypertension

Key facts

Where
Durham, United StatesSee the site
Phase
Phase 4

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT04454203, who can take part

Where in United States

  • Duke University HospitalDurham, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Duke University
Trial code
NCT04454203
Record updated
23 March 2026
Original description
The goal of this prospective randomized double-blind study is to determine if an ultrasound guided peri-arterial injection of local anesthetic (LA) superomedially the femoral artery via peripheral nerve catheter reverses ischemic hypertension associated with prolonged lower extremity tourniquet time.Read full original descriptionShow less

Femoral Peri-arterial Local Anesthetic Injection Via Peri-arterial Perineural Catheter Reverses Tourniquet Associated Ischemic Hypertension

The goal of this prospective randomized double-blind study is to determine if an ultrasound guided peri-arterial injection of local anesthetic (LA) superomedially the femoral artery via peripheral nerve catheter reverses ischemic hypertension associated with prolonged lower extremity tourniquet time.

Inclusion: Patients that will be included in the study are English speaking 18-75 year old ASA 1-3 patients undergoing total ankle arthroplasty.

Exclusion: Pregnant women (as determined by standard of care day-of surgery urine bHCG); Suspected, or known addiction to or abuse of illicit drug(s), prescription medicine(s), or alcohol within the past 2 years; Infection at the site of block placement; Intolerance/allergy to local anesthetics; Uncontrolled anxiety, schizophrenia, or other psychiatric disorder that, in the opinion of the investigator, may interfere with study assessments or compliance; Current or historical evidence of any clinically significant disease or condition that, in the opinion of the investigator, may increase the risk of surgery or complicate the subject's postoperative course; Age under 18 years old or greater than 75 years old; ASA 4 or 5; Diagnosis of chronic pain; Daily chronic opioid use (over 3 months of continuous opioid use); Inability to communicate pain scores or need for analgesia; Weight <50 kg.

ClinicalTrials.gov NCT04454203