Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
60 participants
INTERVENTIONAL
2012-03-31
2012-10-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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control
Patients received intravenously saline solution at 5 ml/Kg/h
No interventions assigned to this group
dopamine
Patients received intravenously saline solution at 5 ml/Kg/h and dopamine at 3 mcg/Kg/min
Dopamine
crystalloids
Patients received intravenously saline solution at 10 ml/Kg/h
No interventions assigned to this group
Interventions
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Dopamine
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* age 24-42
* patients undergoing gynaecological laparoscopy
Exclusion Criteria
* renal and endocrine disorders
* obesity (BMI \> 30 Kg/m2)
* the assumption of drugs that could interfere with renal parameters considered in the study
24 Years
42 Years
FEMALE
No
Sponsors
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Catholic University of the Sacred Heart
OTHER
Responsible Party
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Francesca Bevilacqua
Medical Doctor
Locations
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Catholic University of the sacred Heart
Rome, Rome, Italy
Countries
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Other Identifiers
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FRF-2012-DH
Identifier Type: -
Identifier Source: org_study_id