Ketamine Infusion for Postpartum Depression and Pain

Ketamine Pharmacokinetics and Pharmacodynamics for Postpartum Depression and Pain After Cesarean Delivery

Recruiting Phase 1 Interventional Study
Pain Postpartum Depression
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Other
Participants needed
50 (estimated)
Sponsor
University of Utah · Other
Who this trial is looking for

This trial is looking for women who have just had a cesarean delivery and are experiencing pain or postpartum depression. Participants will receive ketamine infusions to help understand how it works in their body compared to others.

Are You a Good Fit for This Trial?
Must not be taking KetaminePCPLithiumValproateCarbamazepineLamotrigine
Rules you out Preterm deliveryPsychosisSchizophreniaActive abuse of ketamine or PCP

You may be able to join if

  • I am an adult 18 years or older
  • I have had a cesarean delivery
  • I am not planning to breastfeed or need ketamine for pain management
  • I am at least 37 weeks pregnant when I deliver
  • I can provide informed consent
  • I am ASA PS 2 or 3

You may not be able to join if

  • I had general anesthesia for my cesarean delivery
  • I am allergic to ketamine
  • I have a history of schizophrenia or psychosis
  • I have uncontrolled hypertension, chest pain, or arrhythmias
  • I have liver or renal insufficiency
  • I was previously in another pain or depression trial
  • I cannot participate in study procedures for any reason
  • I have a severe pre-eclampsia

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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About This Trial
The purpose of this study is to identify pharmacokinetics of postpartum ketamine infusion. This study will assess ketamine kinetics and metabolism in this setting. Ketamine is expected to exert different kinetics during the physiologic state of post-pregnancy. The goal in conducting this study is to better understand the pharmacokinetics and pharmacodynamics of postpartum ketamine infusion. A seco…
Trial Locations
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Eligibility Criteria
Peripartum Participants: Inclusion Criteria * Cesarean delivery * Adults 18 years and older * Term delivery ≥ 37 weeks gestation anticipated at time of delivery * ASA PS 2 or 3 * Able to provide informed consent * One of the following must be met for inclusion: Not planning to breastfeed OR ketami…
Contacts

Natalie Bennion, MPH

385-209-1185

natalie.bennion@utah.edu

CONTACT

Amy Monroe, MPH, MBA

412-609-6161

a.monroe@utah.edu

CONTACT