F43.0 I10.0
Conditions
Interventions
Group 1: Clinical Trial - To determine how much stress within surgery affects the duration of an operation. For this, the surgeons are asked about their stress levels before and after the operation an
Sponsors
Bundeswehrkrankenhaus Ulm
Eligibility
Sex/Gender
All
Age
25 Years to 65 Years
Inclusion criteria
Inclusion criteria: Surgeon is a specialist in orthopedics and traumatology Assistant at least continuing education assistant for surgery - including doctor
Exclusion criteria
Exclusion criteria: No more age than 65, electrical cardial devices
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of the study is to be a total of 25 operations, each involving 2 operators. The purpose of the endpoint is to demonstrate measurable differences in heart rate, skin resistance, and cardiac variability as a sign of stress related to certain preoperative stressors, as well as intraoperative stressors. It states that there are measurable differences between well-rested, non-stressed previous days and pers. Findings according to questionnaires are available to stressed operators, as well as differences due to operational events influencing the measured variables. | — |
Secondary
| Measure | Time frame |
|---|---|
| Measurements should be completed in 18 months. This is the secondary endpoint with 18 months duration. Then there is definitely an evaluation | — |
Countries
Germany
Contacts
Public ContactKevin Dallacker-Losensky
Bundeswehrkrankenhaus Ulm
Outcome results
None listed