Status:
COMPLETED
Combined Colloids And Crystalloids Versus Crystalloids in Women With Preeclampsia Undergoing Cesarean Delivery
Lead Sponsor:
Mansoura University
Conditions:
Pre-Eclampsia
Cesarean Section
Eligibility:
FEMALE
19-40 years
Phase:
NA
Brief Summary
This study will compare between combination of colloids/crystalloids and crystalloids in women with preeclampsia undergoing elective cesarean delivery under spinal anesthesia
Detailed Description
This randomized, controlled, double blind study will be conducted on women with preeclampsia with singleton pregnancy undergoing elective cesarean delivery under spinal anesthesia. Immediately, after ...
Eligibility Criteria
Inclusion
- Preeclampsia: Blood Pressure ≥140/90 mmHg after 20 weeks' gestation and proteinuria ≥300 mg/24 hours or 1+ on urine dipstick
- Singleton pregnancy
- Elective cesarean delivery under spinal anesthesia
Exclusion
- Height \<150 cm
- Weight \<60 kg
- Body mass index ≥45 kg/m2
- Women presenting in labor
- Contraindications to spinal anesthesia (increased intracranial pressure or local skin infection)
- Diabetes mellitus, cardiovascular, cerebrovascular, or renal disease
- Preoperative administration of intravenous hydralazine or magnesium sulphate
- Hemoglobin \<10 gm/dL
- International Normalized Ratio \>1.3
- Platelet count \<100,000 /mm3
- Preoperative serum creatinine \>1.1 mg/dL
Key Trial Info
Start Date :
August 19 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 15 2021
Estimated Enrollment :
140 Patients enrolled
Trial Details
Trial ID
NCT03252496
Start Date
August 19 2017
End Date
July 15 2021
Last Update
September 5 2021
Active Locations (1)
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1
Department of Anesthesia, Mansoura University Hospitals
Al Mansurah, Dakahlia Governorate, Egypt, 35511