Kuopio University Hospital
Kuopio, Northern Savonia, 70029, Finland
NCT Number: NCT02571179
Physiological changes during pregnancy are known to affect the pharmacokinetics of many drugs. Intranasal fentanyl is an interesting option for obstetric analgesia, but its use in pregnant patients has not been established. The investigators studied pharmacokinetics of intranasal fentanyl in labouring women and to subsequently evaluate the maternal and fetal safety after administration.
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Notify Me18 year–45 year
Female
Interventional
Phase 4
Kuopio, Northern Savonia, 70029, Finland
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Not agreed to participate
When contraction pain was ≥ 5/10 (numerical rating scale 0= no pain, 10= worst pain), the parturient was given a intranasal fentanyl 50 µg dose. After 15 minutes, if contraction pain was still ≥ 5/10, a second 50 µg intranasal dose was administered. Fentanyl was administered every 15 minute until contraction pain decreased to less than 5/10 or until the maximum fentanyl dose of 250 µg was administered.
Time frame: From the first intranasal fentanyl dose to birth of the newborn up to 48 hours
Kuopio University Hospital
Other
Intranasal Fentanyl in Treatment of Labour Pain - Efficacy and Safety
Acronym: fentaobs
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