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Dose Low Dose Ketamine in Casesarian

NCT06237569 · Inonu University

Closed to entry
Status
Not accepting participants
Not applicable
Phase
150
Target enrolment
1
Study sites
Outside the US

What it is testing

Summary

The results of ketamine, ketamine and midazolom and placebo can be copied after birth in cesareans subjected to spinal anesthesia.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • postpartum depression

    Measured over 4 weeks

  • intraoperative complications

    Measured over 1 day

  • postoperative pain

    Measured over 1 day

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years to 45 Years
Ages
FEMALE
Sex
Accepted
Healthy volunteers
Inclusion Criteria: American Society of Anesthesiologists 2-.3 18 -45years old Patients planned to be born by cesarean section The patient requests a cesarean section with spinal anesthesia ExclusionCriteria: Pathological obstetric complications Hypertension Contraindication for ketamine Contraindication for spinal

Where

1 study site

FacilityCityRegionCountry
Inonu universitesiMalatyaTurkey (Türkiye)

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT06237569 on ClinicalTrials.gov →

Last updated in the registry 2024-02-01. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits