Caffeine and Prophylactic Noradrenaline Requirement During Cesarean Delivery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-40
SponsorCairo University

About this trial

Spinal anesthesia is the preferred regional technique in obstetric practice because it provides high maternal satisfaction and eliminates the need for airway manipulation. Despite these advantages, it is frequently complicated by spinal anesthesia-induced hypotension , defined as a reduction in systolic blood pressure of more than 20% from baseline or an absolute SBP below 100 mmHg. Spinal hypotension can have serious consequences, including maternal hypoperfusion that may lead to neurological or renal dysfunction, as well as fetal acidosis and bradycardia, which can compromise neonatal outcomes. The present study aims to evaluate the effect of preoperative caffeine administration on noradrenaline requirements during spinal anesthesia in obstetric patients. Specifically, the objectives are to compare noradrenaline requirements between the study groups and to assess the incidence of hypotension in both groups.

Eligibility criteria

Qualifiers

Full-term singleton pregnant (>37 weeks)

ASA II

undergoing elective cesarean section.

Disqualifiers

Patient refusal

SBP < 100 mmHg

Allergy to local anesthetics or caffeine

Coagulopathy (INR>1.4 or platelets <75.000)

Trial design

Treatments tested in this trial

  • Caffeine (200 mg)
  • Placebo

Treatment groups

62 Participants
are divided into 2 treatment groups

Sponsors and collaborators