Indication for Intraoperative Volume Therapy

This study evaluates which substitution solutions are used in daily clincal practice in various teaching hospitals in a specific district (Frankfurt/Rhine-Main Metropolitan Region). Furthermore the indication for usage of these solutions is investigated.

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Key information

Conditions

Patients Undergoing Any Kind of Surgery

Sex eligibility

All sexes

Study type

Observational

Primary location

Goethe University Hospital

Frankfurt am Main, Hesse, 60590, Germany

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

patients undergoing surgery receiving at least one bag of cristalloid or colloid solution

Exclusion criteria

decline of participation

Treatment and study plan

Primary outcomes

Number of Different Substitution Solutions Administered

Time frame: 24h

Sponsors and collaborators

Lead sponsor

Johann Wolfgang Goethe University Hospital

Other

Registry information

Acronym: INDIZ_IV_I

Important dates

Study start: 2011
Primary completion: 2012
Study completion: 2013
First posted: Oct 18, 2011
Registry last updated: Sep 14, 2017

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.