Overview
Dexmedetomidine and Midazolam Nebulization as Sedation During Cesarean Delivery in Pre-eclampsia
Status:
Recruiting
Recruiting
Trial end date:
2022-01-30
2022-01-30
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
Null hypothesis: There is no difference between the effects of nebulization of dexmedetomidine and midazolam as procedural sedation during cesarean delivery under spinal Anesthesia in pre-eclamptic parturients Alternative hypothesis: There is difference between the effects of nebulization of dexmedetomidine and midazolam as procedural sedation during cesarean delivery under spinal anesthesia in pre-eclamptic parturientsPhase:
Phase 2Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Zagazig UniversityTreatments:
Dexmedetomidine
Midazolam
Criteria
Inclusion Criteria:- Age: 21-38 years old.
- Mild and moderate preeclampsia parturient.
- American Society of AnesthesiologistPhysical status II.
- Body Mass Index (BMI) (25-35kg/m²).
- Type of operations: elective cesarean section under spinal anesthesia.
- Written informed consent from the parturient.
Exclusion Criteria:
- Altered mental state.
- Women with known history of allergy to study drugs.
- Women with uncontrolled diabetes mellitus, bleeding, coagulation disorders, advanced
hepatic, renal, cardiovascular, respiratory disease and neuropsychiatric disorders.
- Patients receiving anticonvulsants or antidepressants.
- Sever preeclampsia, intrauterine growth restriction or fetal compromise.