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NCT07343843

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

Recruiting now NA Last updated 21 January 2026
What this trial tests

NA trial testing Dexmedetomidine in Virtual Reality in 52 participants. Currently enrolling.

Timeline
17 January 2026
Primary endpoint
1 July 2026
1 July 2026

Quick facts

Lead sponsorBenha University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment52
Start date17 January 2026
Primary completion1 July 2026
Estimated completion1 July 2026
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Benha University

Who can join

18 and older, female only, with Virtual Reality or Dexmedetomidine. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Dexmedetomidine

Trials testing the same drug.

Other recruiting trials for Virtual Reality

Currently open trials in the same condition.

Other Benha University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07343843.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing