NL-OMON32311CompletedPhase 3
Differences in maternal temperature and saturation after administration of remifentanil PCA or epidural analgesia during labor - maternal temperature and oxygen saturation during delivery
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Enrollment
- 175
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 to 99 (—)
Inclusion Criteria
- •* Age *18 years
- •* Between 37-42 weeks of gestation
- •* Singleton pregnancy
- •* ASA physical status I or II
Exclusion Criteria
- •* Prior administration of regional of opioid analgesia (during this delivery).
- •* Morbid obesity (BMI * 40 kg/m2)
- •* Drug allergy: history of hypersensitivity to opioid or local anesthetic substances
- •* High risk pregnancy: including severe asthma (daily use of medication), insulin dependent diabetes, severe pre-eclampsia (proteinuria * 5 grams)
- •* Use of antibiotics during delivery
- •* Initial maternal SpO2 of less than 98%
- •* Initial maternal temperature of 38°C or higher.
- •* Cervical dilation of > 7 cm
- •* Ruptured membranes for more than 24 hours at time of inclusion
- •* Contraindication for epidural analgesia
Investigators
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