Patient Satisfaction With Virtual Postoperative Visit

Completed · Not applicable

Conditions studied: Post-Op Complication

In brief

This is a prospective, randomized study designed to evaluate the effects of different initial postoperative follow-up modalities. Given the nature of the study, it is not possible for either the surgeons or the subjects to be blinded. To reduce bias that may occur due to each surgeon's personal preference for postoperative follow-up modality, the surgeons (rather than individual subjects) will be randomized to one of two postoperative follow-up modality groups (traditional or virtual).

Key facts

Study ID
NCT04108442
Run by
NYU Langone Health
People needed
122
Starts
2019-08-01
Expected to finish
2020-03-01
Last updated by the study team
2020-10-09

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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