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Comparison of Telemedicine Evaluation to Standard Evaluation Methods for Pre-Anesthesia Consultation

Comparison of Telemedicine Evaluation to Standard Evaluation Methods for Pre-Anesthesia Consultation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01240239
Enrollment
200
Registered
2010-11-15
Start date
2010-01-31
Completion date
2013-09-30
Last updated
2016-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ENT Patients Scheduled for Surgery

Keywords

Pre anesthesia consultation, telemedicine

Brief summary

The purpose of the study is to evaluate different methods of pre-anesthesia consultation, with the aim of improving the day of surgery experience for the patient. In this study, we will use a telephone consultation, an in-person consultation, and a telemedicine consultation, which involves television cameras and monitors that allow live two-way communication for the pre-anesthesia consultation. The reason for this study is to evaluate the use of telemedicine for the pre-anesthesia consultation. Patients and anesthesiologists have been highly satisfied in previous studies using pre-anesthesia telemedicine consultation. In this study, we will examine a larger group of patients, as previous studies have studied smaller groups of patients.

Interventions

None listed

Sponsors

Loma Linda University
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* Patients between the ages of 18 and 89 who are scheduled for otolaryngologic procedures and pre-anesthesia consultation.

Exclusion criteria

Lack of consent; inability to understand English-

Design outcomes

Primary

MeasureTime frameDescription
Comparison Of Telemedicine Evaluation To Standard Evaluation Methods For Pre-Anesthesia Consultationabout 1 monthPrimary outcomes include surgical cancellation rate, delays the day of surgery secondary to inadequate pre-op evaluation, adequacy of the airway, respiratory, and cardiovascular exams, and intra-op and post-op complications. Patient data will include age, gender, ASA Physical Status and type of surgery. The length of the PACE appointment and the number of days prior to surgery the PACE appointment was conducted will be noted. Patient satisfaction with the will be evaluated.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026