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临床试验/NCT06237569
NCT06237569尚未招募不适用

Effects of Low Dose ketamıne on Postpartum Depression During Caesarean Sections

Inonu University1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2024年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
入组人数
150
试验地点
1
主要终点
postpartum depression

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 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

排除标准

  • 未提供

研究组 & 干预措施

Grup 1 -Ketamine Group

Ketamine Group (GROUP 1) 0.5 mg/kg IV single dose bolus diluted to 5 ml with 0.9% saline

干预措施: Application of ketamine and midazolam or ketamine alone to patients undergoing cesarean section under spinal anesthesia (Drug)

Group 2-ketamine + midazolam

Midazolam 0.0125 mg/kg is given followed by a single IV bolus dose of 0.5 mg/kg diluted to 5 ml with 0.9% saline.

干预措施: Application of ketamine and midazolam or ketamine alone to patients undergoing cesarean section under spinal anesthesia (Drug)

Group 3-placebo

Group 3-placebo ;A single dose of IV 5 ml physiological saline will be given.

干预措施: Application of ketamine and midazolam or ketamine alone to patients undergoing cesarean section under spinal anesthesia (Drug)

结局指标

主要结局

postpartum depression

时间窗: 4 weeks

Reducing postpartum depression with low-dose ketamine

intraoperative complications

时间窗: 1 day

Reducing postpartum depression by reducing ketamine-related intraoperative complications

postoperative pain

时间窗: 1 day

Reducing postoperative pain with low dose ketamine

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

DUYGU DEMİROZ

principal investigator

Inonu University

研究点 (1)

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