Effect of Different Administration Routes of Dexmedetomidine Combined with Ultrasound-Guided Fascia Iliaca Block on Emergence Agitation After Hip Replacement Surgery

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-65
SponsorQianfoshan Hospital

About this trial

To examine the impact of various administration routes of dexmedetomidine in conjunction with ultrasound-guided fascia iliaca block (FIB) on emergence agitation (EA) during the postoperative recovery period after hip replacement surgery.

Eligibility criteria

Qualifiers

age between 18 and 65 years, with no restriction on gender

diagnosis of hip joint disease necessitating hip arthroplasty

ASA grade I-II

no significant cardiopulmonary, hepatic, or renal dysfunction prior to the operation

Disqualifiers

patients allergic to or with contraindications to ropivacaine or dexmedetomidine

patients exhibiting symptoms of agitation or delirium prior to the procedure

patients with severe central or peripheral nervous system disorders

patients with coagulation disorders or receiving anticoagulant therapy

Trial design

Treatments tested in this trial

  • Dexmedetomidine Injection
  • Ropivacaine and Dexmedetomidine
  • Sodium Chloride Injection

Treatment groups

207 Participants
are divided into 3 treatment groups

Sponsors and collaborators