NCT06093750 is a clinical trial in Preoperative Vegetative Stress, sponsored by Ludwig Boltzmann Institute for Traumatology - The research center in cooperation with AUVA.

What condition does NCT06093750 study?

NCT06093750 studies Preoperative Vegetative Stress.

Is NCT06093750 still recruiting?

NCT06093750 is currently completed. Last updated 23 October 2023.

Last reviewed 2023-10-23 · How we verify

NCT06093750

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

Correlation Between State-Trait-Anxiety-Inventory and Heart Rate Variability

Completed Last updated 23 October 2023

What this trial tests

trial in Preoperative Vegetative Stress in 50 participants. Completed in 2 October 2023.

Timeline

5 June 2023

Primary endpoint
30 September 2023

2 October 2023

Quick facts

Lead sponsor	Ludwig Boltzmann Institute for Traumatology - The research center in cooperation with AUVA
Status	Completed
Study type	OBSERVATIONAL
Enrollment	50
Start date	5 June 2023
Primary completion	30 September 2023
Estimated completion	2 October 2023
Sites	1 location across Austria

Conditions studied

Preoperative Vegetative Stress — all drugs for Preoperative Vegetative Stress →

Sponsor

Ludwig Boltzmann Institute for Traumatology - The research center in cooperation with AUVA

Who can join

Adults 18 to 65, any sex, with Preoperative Vegetative Stress. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the study is to investigate whether there is a correlation between the vegetative stress evaluated by the State-Trait-Anxiety-Inventory (STAI-Test) and the measurement of heart rate variability (HRV). A subgroup analysis will also be performed to determine whether premedication contributes to a lower STAI score and/or heart rate variability. The primary outcome will be the parameter of frequency-based analysis Low Frequency (LF) and High Frequency (HF), and the STAI score. Secondary outcomes are the parameters Low Frequency/High Frequency-ratio (LF/HF-ratio), Standard deviation of normal-to-normal (NN) intervals (SDNN), Root Mean Square of successive differences" (RMSSD) and mean heart rate, age, gender, if they are smokers and if they work in shifts.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other Ludwig Boltzmann Institute for Traumatology - The research center in cooperation with AUVA trials

Trials by the same sponsor.

NCT05895253 — Safety and Efficacy of Vibro-tactile Feedback for Patients Who Underwent Lower Limb Amputation · NA · terminated

Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT06093750 (US National Library of Medicine, public domain)
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Ludwig Boltzmann Institute for Traumatology - The research center in cooperation with AUVA
Last refreshed: 23 October 2023

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06093750.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing