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OpenTrials
Completed

NCT Number: NCT00222391

Influence of Thoracic Epidural Anesthesia on Skin Sympathetic Activity and Heart Rate Variability

The purpose of the study is to evaluate the impact of epidural anesthesia on sympathetic activity in surgical patients. The study investigates whether a segmental sympathetic block can be determined and can be correlated to level of the sensoric blockade.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Anesthesia and Intensive Care, University Hospital Muenster

Münster, D-48149, Germany

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • elective surgery
  • combined anesthesia with thoracic epidural anesthesia 8 (Th6-9
  • Body-mass-index < 30

Exclusion criteria

  • Fever, Hypothermia, SIRS
  • Microangiopathy
  • Neuropathy
  • Sensomotoric deficits

Treatment and study plan

Primary outcomes

  1. Hemodynamic parameters

Secondary outcomes

  1. Level of sensoric block

  2. skin temperature

Sponsors and collaborators

Lead sponsor

University Hospital Muenster

Other

Registry information

Official study title

Influence of Thoracic Epidural Anesthesia on Skin Sympathetic Activity and Heart Rate Variability in Surgical Patients

Important dates

Study start
2004
Study completion
2006
First posted
Sep 22, 2005
Registry last updated
Jan 7, 2009

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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