In this study the analgesic effect of two different opioids (fentanyl and sufentanil) will be
compared when given either intrathecally or epidurally in primiparous parturients during
early phase of the labour.
Drug: Spinal analgesia for labour pain
Drug: Epidural analgesia for labour pain
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Locations near you
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Full eligibility criteria for NCT02885350
Ages eligible for Study
18 Years to 45 Years
Genders eligible for Study
Accepts Healthy Volunteers
In early phase of labour (cervical dilatation at or under 5 cm)
No prior opioids by any route of administration within past 120 min
Pain at or over 80 mm on 0-100 mm visual analog scale during contraction
Allergy for any of the medications used
Contraindications for epidural/spinal analgesia
BMI at the time of delivery under 20 or over 35 kg/m2
All locations for NCT02885350
Maternity Hospital, Helsinki University Central Hospital
Helsinki, Uusimaa, Finland, FI-00610
not yet recruiting
View full eligibility
Tris trial is registered with FDA with number: NCT02885350. The sponsor of the trial is Helsinki University Central Hospital and it is looking for 80 volunteers for the current phase.
Official trial title: Spinal or Epidural Fentanyl or Sufentanil for Labour Pain in Early Phase of the Labour
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