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Clinical Trials/KCT0007959
KCT0007959Recruiting未知

Evaluation of analgesic effects of ultrasound-guided pericapsular nerve group (PENG) block combined with lateral femoral cutaneous nerve (LFCN) block in total hip replacement arthroplasty under spinal anesthesia

Samsung Medical Center0 sites82 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
未知
Status
Recruiting
Enrollment
82

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional Study

Eligibility Criteria

Ages
20(Year) to 70(Year) (—)
Sex
All

Inclusion Criteria

  • Adults between 20 and 70 years of age
  • - Patients undergoing THA
  • - ASA physical status I,II : ex) Healthy adult without underlying disease (I), patient with systemic disease such as controlled hypertension or controlled diabetes, but can be controlled with medication or surgical treatment (II)

Exclusion Criteria

  • - ASA physical status III or higher
  • - Pregnant
  • - Patients with severe blood clotting disorders (last INR over 1.5 before surgery)
  • - Patients with cerebrovascular disease
  • - Systemic infection, patients with infection at the site of nerve block
  • - Patients with chronic pain disorder or neurological disorder
  • - Patients allergic to local anesthetics
  • - Patients who did not understand this study and expressed their intention not to participate in the study
  • - Patients who have communication problems or cannot express the severity of their pain

Investigators

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