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Dose Low Dose Ketamine in Casesarian

Effects of Low Dose ketamıne on Postpartum Depression During Caesarean Sections

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06237569
Enrollment
150
Registered
2024-02-01
Start date
2024-06-01
Completion date
2024-09-01
Last updated
2024-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain, Postpartum Depression

Keywords

midazolam with low dose ketamine, low dose ketamine, postoperatıve analgesıc need, postpartum depression

Brief summary

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

Detailed description

Postpartum depression will be evaluated by dividing the patients into 3 groups: group 1 as ketamine, group 2 as ketamine and midasom, and group 3 as placebo group.

Interventions

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

A single dose of 0.5 mg/kg IV diluted to 5 ml with 0.9% saline was planned to be administered simultaneously to the Ketamine Group (GROUP 1), ketamine and midazolam within 5 minutes after the newborn umbilical cord was clamped (Group 2). After midazolam 0.03 mg/kg is given, a single dose IV bolus of 0.5 mg/kg diluted to 5 ml with 0.9% saline will be administered. Patients experience dizziness, hallucinations, nausea, headache, vomiting, diplopia and blurred vision, the time until the first analgesic request; Depression parameters will be evaluated with the Edinburgh Postpartum Depression Scale (EPDS) in all patients before cesarean section and at the 1st, 2nd and 4th weeks after birth.

Sponsors

Inonu University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
postpartum depression4 weeksReducing postpartum depression with low-dose ketamine
intraoperative complications1 dayReducing postpartum depression by reducing ketamine-related intraoperative complications
postoperative pain1 dayReducing postoperative pain with low dose ketamine

Countries

Turkey (Türkiye)

Contacts

Primary ContactDUYGU DEMIROZ, dr
drduygudemiroz@hotmail.com+905319504421
Backup ContactOSMAN TOPLU, dr
osman.toplu@inonu.edu.tr905321137771

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026