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Renal Function During Laparoscopic Surgery

Information source: Catholic University of the Sacred Heart
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Intra Operative Fluid Management

Intervention: Dopamine (Drug)

Phase: N/A

Status: Completed

Sponsored by: Catholic University of the Sacred Heart

Summary

Aim of this study was to investigate the cardiac and renal responses to the administration of different amount of crystalloids, with and without dopamine, during gynaecological laparoscopic surgery.

Clinical Details

Official title: Dopamine Infusion and Crystalloids Administration Improve Renal Function During Laparoscopic Surgery

Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Primary outcome: estimated glomerular filtration rate, tissue Doppler imaging, E/Ea

Secondary outcome: total intra operative diuresis (TID)

Eligibility

Minimum age: 24 Years. Maximum age: 42 Years. Gender(s): Female.

Criteria:

Inclusion Criteria:

- ASA I

- age 24-42

- patients undergoing gynaecological laparoscopy

Exclusion Criteria:

- cardiovascular diseases

- renal and endocrine disorders

- obesity (BMI > 30 Kg/m2)

- the assumption of drugs that could interfere with renal parameters considered in the

study

Locations and Contacts

Catholic University of the sacred Heart, Rome 00168, Italy
Additional Information

Starting date: March 2012
Last updated: November 5, 2012

Page last updated: August 23, 2015

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