Actively Recruiting
Virtual Reality Versus Intravenous Dexmedetomidine on Maternal Anxiety, Stress, Hemodynamics, and Neonatal Outcomes During Cesarean Section
Led by Benha University · Updated on 2026-01-21
52
Participants Needed
1
Research Sites
23 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Virtual Reality Versus Intravenous Dexmedetomidine on Maternal Anxiety, Stress, Hemodynamics, and Neonatal Outcomes During Cesarean Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years old.
- American Society of Anesthesiologists (ASA) physical status II.
- Scheduled for elective cesarean section delivery under Central Neuraxial Blockade.
- Provide informed consent and agree to participate in the study.
You will not qualify if you...
- Patient's refusal.
- Contraindications for Regional Anesthesia such as infection at the injection site, severe coagulopathy, or allergy to local anesthetics.
- Psychiatric disorders.
- Sensory impairment like blindness or deafness.
- Any technical problem preventing proper fitting of VR glasses.
- Cognitive impairment, epilepsy, or claustrophobia.
- Suspected eye infection.
- Signs of active labor.
- Pregnancy-related diseases or antepartum hemorrhage.
- Presence of fetal distress.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Benha University
Banhā, Benha, Egypt, 13518
Actively Recruiting
Research Team
E
Emad M Sayed, MBBCH
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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