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Clinical Trial Summary

This will be a parallel design, nonblinded, randomized controlled superiority trial investigating the utility of a virtual reality (VR) experience to provide analgesia for external cephalic version (ECV).


Clinical Trial Description

Subjects will be: Pregnant women, age >18 years, with a singleton pregnancy at >36 weeks gestational age, healthy (American Society of Anesthesiologists physical status class II), with an otherwise uncomplicated pregnancy (i.e. no fetal abnormalities or significant maternal morbidity, scheduled for ECV at Columbia University Irving Medical Center (CUIMC) with a plan to receive no anesthesia for the procedure. Patients will be randomly assigned to either the VR or No VR group. The intervention will be provided for the duration of the ECV procedure (typically 15 - 30 mins). ;


Study Design


Related Conditions & MeSH terms

  • Analgesia Management for External Cephalic Version

NCT number NCT03588182
Study type Interventional
Source Columbia University
Contact
Status Terminated
Phase N/A
Start date May 18, 2019
Completion date December 6, 2023