Neuraxial Preservative Free Morphine for Normal Spontaneous Vaginal Delivery

  • STATUS
    Recruiting
  • End date
    Dec 25, 2021
  • participants needed
    140
  • sponsor
    Icahn School of Medicine at Mount Sinai
Updated on 25 January 2021
morphine
vaginal delivery

Summary

Patients presenting for normal spontaneous vaginal delivery who have a neuraxial anesthestic will be randomized to receive preservative free morphine or saline placebo after delivery.

Description

After obtaining consent, women presenting to the labor floor at Mount Sinai Hospital will be randomized into two groups, intervention and placebo. Baseline demographic data and surveys in regards to postpartum depression, anxiety, breastfeed willingness and pain scores will be obtained. After delivery of the baby patients will either receive 2mg preservative free morphine or saline via the epidural catheter prior to its removal. The study team will then record pain and recovery scores, as well as follow up screens to the aforementioned endpoints. The study will end at the 6 week postpartum visit with the patient's obstetrician.

Details
Condition Postpartum depression, Post-Partum Depression, Opioid Consumption, Postpartum Pain
Treatment Saline, Preservative Free Morphine
Clinical Study IdentifierNCT04017442
SponsorIcahn School of Medicine at Mount Sinai
Last Modified on25 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Pregnant women in labor

Exclusion Criteria

Not a candidate for neuraxial anesthesia
Patient refusal
Allergy to morphine
Patients with chronic pain syndromes
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