Quality of Postoperative Analgesia and Functional Recovery After Elective Cesarean Delivery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorEnte Ospedaliero Cantonale, Bellinzona

About this trial

Based on randomization, patients will receive a mixture for spinal anesthesia and will be followed in the following hours for the various outcomes and for functional recovery

Eligibility criteria

Qualifiers

patients over 18 year of age

height over 160 cm

American Society Anesthesiologists physical status I and II

term singleton parturients

Disqualifiers

patients with inability to consent

patient refusal

contraindication to spinal anesthesia (eg, hemodynamic instability, infection at the surgery site, and neurologic defects such as transverse myelitis)

emergency cesarean delivery

Trial design

Treatments tested in this trial

  • Fentanyl 1
  • Fentanyl2
  • Fentanyl 3

Treatment groups

63 Participants
are divided into 3 treatment groups