Phase
Condition
Acute Pain
Treatment
Saline solution (placebo)
Intrathecal morphine
Clinical Study ID
Ages 18-50 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adult (≥18 years) term primiparous (≥37 weeks) patients with live singletonpregnancy
Patients who request labour analgesia and do not have any contraindications forneuraxial analgesia.
Less than or equal to 6 cm cervical dilation during the last vaginal examination.
Exclusion
Exclusion Criteria:
Patients who are expected to be discharged within 24 hours of delivery.
Patients with chronic pain conditions, opioid use disorder, pre-gestationaldiabetes, obstructive sleep apnea, morbid obesity (BMI >40 kg/m2), or fetalabnormalities.
Patients who have intramuscular morphine within 12 hours or fentanyl >200 mcg in thepreceding 4 hours.
Participants will be excluded from further analysis in case of spinal analgesicfailure
Participants will be excluded from further analysis if labour lasts less than 2hours
Study Design
Study Description
Connect with a study center
Mount Sinai Hospital
Toronto, Ontario M5G1X5
CanadaActive - Recruiting
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