UnknownN/Aketamine

Dose Low Dose Ketamine in Casesarian

Sponsored by Inonu University

NCT ID
NCT06237569
Target Enrollment
150 participants
Start Date
2024-06-01
Est. Completion
2024-09-01

About This Study

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

Conditions Studied

Postoperative PainPostpartum Depression

Interventions

  • Application of ketamine and midazolam or ketamine alone to patients undergoing cesarean section under spinal anesthesia

Eligibility

Sex:FEMALE
Age:18 Years - 45 Years
Healthy Volunteers:Yes
View full eligibility criteria
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

Study Locations (1)

Inonu universitesi
Malatya, Turkey (Türkiye)

This trial is not recruiting

This study is currently not accepting new participants.

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Data Source
ClinicalTrials.gov

Last updated from source

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