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临床试验/NCT06221280
NCT06221280Enrolling By Invitation不适用

Effects of Transversus Abdominis and Erector Spina Plane Blocks on Post-Cesarean Pain Control and Postpartum Depression

Kahramanmaras Sutcu Imam University2 个研究点 分布在 2 个国家目标入组 60 人开始时间: 2023年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
60
试验地点
2
主要终点
Pain (VAS score)

研究概览

简要总结

At the end of your cesarean section surgery, which is started by applying medication to the spinal cavity from your waist, pain medication will be applied between the relevant muscle and its covering from your lower abdomen or back with the help of ultrasonography and a special block needle. Then, a patient-controlled pain device with a serum containing painkillers will be connected to your vascular access, and its use and purpose will be explained to you. You will be asked about your pain condition and the severity score of your pain, if any, at certain hourly intervals. At the end of 24 hours, a pain device will be removed, your satisfaction will be questioned and your complaints, if any, will be recorded. Immediately before surgery and 4-6 days after your surgery. An evaluation survey consisting of 10 questions will be asked to you within a 5-minute period during the weeks, at a time when you are free, and your answers will be recorded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • Having a good mental status,
  • Those aged ≥18 years,
  • Term pregnant (gestational age ≥ 36 weeks),
  • American Society of Anesthesiologists class II-III,
  • Patients who underwent cesarean section with spinal anesthesia will be included.

排除标准

  • Having labor at term or obstetric emergency,
  • Having a twin pregnancy,
  • Having a diagnosed psychiatric disorder/using psychiatric medication,
  • Those who are allergic to local anesthetics and/or drugs used in the study,
  • The patient-controlled anesthesia device is out of use for any reason within the first 24 hours postoperatively,
  • Having peripheral neuropathy or neuromuscular disease,
  • Patients using anticoagulant drugs that will prevent regional anesthesia will be excluded from the study.

结局指标

主要结局

Pain (VAS score)

时间窗: 12 months

Evaluation of the postoperative analgesic effectiveness of erector spinae and transversus abdominis plane blocks after cesarean section

次要结局

  • Postpartum depression (Edinnburg Depression Scale)(12 months)

研究者

发起方
Kahramanmaras Sutcu Imam University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Feyza Calisir

Assistant professor

Kahramanmaras Sutcu Imam University

研究点 (2)

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