Ketamine levels after cesarean birth in people with postpartum depression or pain
About this title
Read the official source — NCT06767566Understand this study
Who could participate?
Listed age limits: from 18 years.
What will I do during this study?
After cesarean delivery, participants in the postpartum group receive a 12-hour ketamine infusion: a one-hour loading infusion followed by an 11-hour maintenance infusion. Healthy control participants receive the same infusion protocol for comparison. The study measures how ketamine is processed in the body.
- Listed locations
- Pittsburgh and 1 more locationSee all locations and recruitment
- Study phase
- Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.
What to know before participating
This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?
Things to check before joining
- Recruitment status
- Recruiting
- Enrollment listed in the registry
- 50
- Sponsor
- University of Utah
- Sponsor type
- University
- Study type
- Drug
- Intervention type
- Drug
- Study phase
- Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.
- Locations
- United States
- Age range
- Over 18 Years
- Official registry ID
- NCT06767566
- Official title
Show the full official title
Ketamine Pharmacokinetics and Pharmacodynamics for Postpartum Depression and Pain After Cesarean Delivery
Recruitment & locations
Pittsburgh · Salt Lake City
Interested in joining this study?
Questions about this study
Who is behind this study?
The study sponsor is University of Utah, a university.
Does this study involve medication?
Yes. The study involves medication, including Ketamine (Ketalar).
Who can participate?
Listed age limits: from 18 years.
Is this study still recruiting?
The registry lists this study as recruiting.
