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Indication for Intraoperative Volume Therapy

Indication for Intraoperative Volume Therapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01454258
Acronym
INDIZ_IV_I
Enrollment
10100
Registered
2011-10-18
Start date
2011-10-31
Completion date
2013-03-31
Last updated
2017-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients Undergoing Any Kind of Surgery

Brief summary

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.

Interventions

None listed

Sponsors

Johann Wolfgang Goethe University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* decline of participation

Design outcomes

Primary

MeasureTime frame
Number of Different Substitution Solutions Administered24h

Countries

Germany

Participant flow

Participants by arm

ArmCount
Cohort
Surgical patients from 10 hospitals over a period of 13 months
10,100
Total10,100

Baseline characteristics

CharacteristicCohort
Age, CustomizedNA years
Sex/Gender, CustomizedNA participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 10,100
serious
Total, serious adverse events
0 / 10,100

Outcome results

Primary

Number of Different Substitution Solutions Administered

Time frame: 24h

Population: Surgical patients from 10 hospitals over a period of 13 months

ArmMeasureValue (NUMBER)
CrystalloidsNumber of Different Substitution Solutions Administered7827 participants
Hydroxyethyl StarchNumber of Different Substitution Solutions Administered1055 participants
Other ColloidsNumber of Different Substitution Solutions Administered221 participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026