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Dexmedetomidine as a Part of General Anesthesia for Cesarean Delivery in Patients with Pre-eclampsia: Efficacy and Fetal Outcome

Not Applicable
Conditions
Pregnancy and Childbirth
Surgery
anesthesia
Anaesthesia
Registration Number
PACTR201706002303170
Lead Sponsor
menoufiya faculty of medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
60
Inclusion Criteria

Patients included were 18-40 years, with gestational age ¿ 34 weeks and have mild pre-eclampsia with a systolic blood pressure < 160 mm Hg and a diastolic blood pressure < 110 mmHg and urinary protein dipstick + or 2+.

Exclusion Criteria

Exclusion criteria included patient refusal to be included in the study, allergy to dexmedetomidine, body mass index >40kg/m2, systemic diseases (cardiac, pulmonary, hepatic, renal, neurological, neuromuscular, diabetes mellitus, anemia, coagulation disorders, bleeding disorders, seizures), HELLP syndrome, patients receiving anticoagulant or antipsychotic drugs, anti-partum hemorrhage, fetal distress and multiple pregnancy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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