Status:
NOT_YET_RECRUITING
Preoperative Oral Midodrine Versus Intraoperative Intravenous Norepinephrine in Preventing Post-spinal Anesthesia Hypotension in Cesarean Section: A Prospective Double-blind Randomized Clinical Trial
Lead Sponsor:
Sohag University
Conditions:
Post Spinal Anesthesia Hypotension
Eligibility:
FEMALE
18-35 years
Phase:
NA
Brief Summary
Neuraxial blockade such as spinal anaesthesia can cause severe hypotension due to pharmacological sympathectomy resulting in potential deleterious consequences for the patient, Prevention of this spin...
Eligibility Criteria
Inclusion
- The study will include 90 adult female patients, 45 in each group (between 18-35 years old).
- patients of ASA physical status class I and class II.
- patients scheduled for elective cesarean section under spinal anesthesia.
Exclusion
- Patient refusal.
- Contraindication to spinal anesthesia .
- Patients known allergic to Midodrine or Norepinephrine.
- Patients with preexisting cardiovascular or cerebrovascular disease.
- Patients with diabetes mellitus.
- Patients with psychiatric disease or on psychiatric treatment.
Key Trial Info
Start Date :
February 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2024
Estimated Enrollment :
90 Patients enrolled
Trial Details
Trial ID
NCT06213935
Start Date
February 1 2024
End Date
November 1 2024
Last Update
January 19 2024
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