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Telemedical Risk Assessment and Preoperative Evaluation (TAPE)

R

RWTH Aachen University

Status

Unknown

Conditions

Patients Undergoing Elective Surgery With Anesthesia

Treatments

Device: TAPE-Software

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to assess the feasibility, patient satisfaction and time saving of a telemedical risk assessment and preoperative evaluation for anesthesia.

Full description

The preanesthesia evaluation and risk assessment is conducted by an anesthesiologist prior to elective surgery. The physician assesses the patient´s medical records and specifies the individual preoperative procedure in order to minimize the perioperative risks. The on-site meeting is often connected with extended travel time and during the COVID-19 pandemic also with an increased infection risk for the patient. This project was initiated to reduce time efforts on patient site and to reduce possible infection risks. The TAPE-software turns every patients home into a remote facility allowing the physician to conduct the preanesthesia evaluation over distance.

Enrollment

100 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≥18 years
  • estimated ASA I/II classification based on the American Society of Anesthesiologists (ASA) classification
  • elective surgery
  • surgery at least 14 days in the future
  • patient access to a Windows-10-based personal computer with webcam

Exclusion criteria

  • language or cognitive barriers (e.g. dementia, laryngectomy...)
  • high risk surgeries with need of postoperative ICU stay
  • acute infection with required auscultation

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

Preoperative evaluation and risk assessment via telemedicine
Experimental group
Treatment:
Device: TAPE-Software

Trial contacts and locations

1

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Central trial contact

Jan Wienhold, cand. med.; Andreas Follmann, Dr.

Data sourced from clinicaltrials.gov

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