Incidence of Pruritus Using Intrathecal Fentanyl Versus Epidural Fentanyl to Initiate Labour Analgesia.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorSt. Justine's Hospital

About this trial

The purpose of this study is to investigate the effect of neuraxial analgesia initiation on the incidence of pruritus in laboring women. Specifically, this study aim to compare intrathecal fentanyl with epidural fentanyl in order to determine whether the epidural route is associated with a lower occurrence and severity of pruritus. By clarifying these differences, the research seek to optimize analgesic strategies during labor while minimizing opioid-related side effects

Eligibility criteria

Qualifiers

Age ≥ 18 years

Vaginal delivery

Gestational age ≥ 37 weeks

Requesting neuraxial analgesia

Disqualifiers

ASA score > 3

Allergy or contraindication to receiving opioids/local anesthesia (morphine or fentanyl)

BMI > 40 kg/m²

Hepatic or renal failure,

Trial design

Treatments tested in this trial

  • Spinal analgesia
  • Epidural Analgesia

Treatment groups

80 Participants
are divided into 2 treatment groups

Sponsors and collaborators