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OpenTrials
Completed

NCT Number: NCT01866137

Copeptin During a Standardized Psychological Stress Test

The aim of the PsyCo Study is to determine whether psychological Stress has an influence on copeptin levels.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital Basel

Basel, Canton of Basel-City, 4031, Switzerland

About this study

healthy volunteers undergo the TSST and stress hormones as cortisol and copeptin are measured

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

•Aged over 18 years

Exclusion criteria

  • Intake of any kind of medication (except birth control pill)
  • BMI >30 kg/m2
  • Evidence of any acute illness
  • History of chronic illness
  • Baseline glucose level >7 mmol/l Baseline sodium level <135 mmol/l or >145 mmol/l

Treatment and study plan

Primary outcomes

  1. Changes in copeptin levels after a psychological stress test in healthy volunteers

    Time frame: 30min before, at time point 0, +10, +20, +40, +60 after the psychological stress test

Secondary outcomes

  1. Changes in copeptin levels after a psychological stress test in patients with central diabetes insipidus

    Time frame: Timpepoint 0, +10, +20, +40, +60 after the psychological stress test

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Registry information

Acronym: PsyCo

Important dates

Study start
2013
Primary completion
2013
Study completion
2014
First posted
May 31, 2013
Registry last updated
Sep 9, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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