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Virtual Reality Versus Intravenous Dexmedetomidine on Maternal Anxiety, Stress, Hemodynamics, and Neonatal Outcomes During Cesarean Section

RecruitingNAAges 18 Years - anyFemaleBenha University
NCT07343843 on ClinicalTrials.gov โ†—
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In plain words

What the trial is, and whether it could suit you

This study aims to compare the efficacy of intravenous dexmedetomidine infusion versus virtual reality (VR) in reducing maternal anxiety, stress, and hemodynamic instability during cesarean section and their effects on neonatal outcome as respiration and heart rate.

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๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Age over 18 years old. * American Society of Anesthesiologists (ASA) physical status II. * Scheduled for elective cesarean section (CS) delivery under Central Neuraxial Blockade. * Provide informed consent and agree to participate in the study. Exclusion Criteria: * Patient's refusal * Patient known have contraindications for Regional Anesthesia as infection at the site of injection, severe coagulopathy or allergy to local anesthetics. * Patient with psychiatric disorders. * Sensory impairment (blindness, deafness). * Any technical problem preventing proper fitting of the glasses to the patient face. * Patients with cognitive impairment, epilepsy or with claustrophobia * Patients with suspected eye infection * Signs of active labor. * Pregnancy related-diseases or antepartum hemorrhage. * Presence of Fetal distress.
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What it tests

  • Dexmedetomidine
  • Virtual reality
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Where

1 site
Benha University
Banhฤ, Egypt
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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