Influence of the timing and quantity of administration of crystalloid fluid on tissue oxygenation in parturients undergoing cesarean section under spinal anesthesia

Not Applicable

Completed

• Conditions: otherwise healthy parturients planned for cesarean section; Anaesthesiology - Other anaesthesiology

• Registration Number: ACTRN12617000758303
• Lead Sponsor: Harran University School of Medicine, Research and Training Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-05-23
• Last Update Posted: 10 August 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

ASA physical status I–II term parturients
undergoing elective CS under spinal anesthesia

Exclusion Criteria

ASA status; > II
Coexisting disease; metabolic, endocrine, hepatic, cardiac or renal diseases, malignancies, preeclampsia; hypertension;
Concurrent medication used; or recent use (within 48h) of any drug with anti-oxidant properties such as nebivolol, carvedilol, vitamins E and C, or acetylcysteine

Study & Design

• Study Type: Interventional
• Study Design: Not specified