The effect of intravenous fluid preload on diuresis during spinal anesthesia-induced detrusor blockade

Status

Not yet recruiting

Phases

Unknown

Study type

Interventional

Source

EU CTR

Registry ID

EUCTR2007-000702-71-NL

Enrollment

150

Registered

2007-07-12

Start date

2007-07-13

Completion date

Unknown

Last updated

2012-03-19

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

Conditions

Diuresis during spinal anesthesia MedDRA version: 9.1 Level: LLT Classification code 10041538 Term: Spinal anesthesia MedDRA version: 9.1 Level: LLT Classification code 10013523 Term: Diuresis

Interventions

Trade Name: HemoHES 6% Pharmaceutical Form: Pharmaceutical form of the placebo: Intravenous infusion Route of administration of the placebo: Intravenous use

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: patients planned for short, minor surgery of lower extremity under spinal anesthesia. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: any urologic, neurologic, cardiac, vascular disease.

Design outcomes

Primary

Measure	Time frame
Main Objective: Determine effects of intravenous fluid preload (given just before spinal anesthesia) on volume of diuresis during spinal anesthesia induced detrusor blockade;Secondary Objective: Determine effects of intravenous fluid preload in preventing hypotension;Primary end point(s): 1) mean volume of diuresis during spinal anesthesia 2) number of subjects with diuresis volume over 500 ml	—

Countries

Netherlands

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026