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临床试验/NCT05843838
NCT05843838招募中不适用

The Effect of Intraoperative Hypotension on Postoperative Cognitive Functions in Cesarean Section Operations

Ankara City Hospital Bilkent1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2024年2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
招募中
入组人数
150
试验地点
1
主要终点
Change in postoperative cognitive function related with hypotension in cesarean section

研究概览

简要总结

The aim of the study is to see whether the hypotension that develops during spinal anesthesia in cesarean section patients causes a decrease in the postoperative cognitive functions of the patient. If the results show a decrease in functions due to the effect of hypotension, it will be necessary to carry out aggressive prevention/treatment of hypotension in cesarean section patients.

详细描述

A total of 150 female patients (75 in each group) between the ages of 18-40 who will undergo caesarean section with spinal anesthesia in the obstetric operating room of Ankara Bilkent City Hospital in ASA 2, 3rd categories will be included in the study.

Patients will be divided into two as hypotensive and non-hypotensive patients in spinal anesthesia with routine doses, and all patients will be given a mini mental test at preop and post op 1st hour. (Hypotension, MAP(mean artery pressure)<65 mmHg, or SAP(systemic arterial pressure) < 30% will be considered as an initial value.) Patients who are hypotensive and need ephedrine will be included in the hypotensive group, and patients without hypotension will be included in the normotensive group. Those with an initial mini mental test score below 24 will not be allowed to study. At the end of the research, the mental test scores of the two groups will be compared and the effect of hypotension will be evaluated.

The patient's name-surname, age, protocol number, indication for cesarean section, method of regional anesthesia applied, sensory block level, Bromage score, side effect follow-up, first ten minutes after the procedure, every two minutes, up to half an hour, and every fifteen minutes after thirty minutes, systolic artery pressure, diastolic artery pressure, average arterial pressure, pulse and ephedrine (if used) will be recorded.

Preoperative, Postoperative first hour Mini Mental Test Score will be administered and recorded

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Female patients between the ages of 18-40 in the ASA2, 3rd categories who will undergo cesarean section with spinal anesthesia who agree to participate in the study

排除标准

  • Failure of the patient to accept
  • The necessity of an additional intervention to the cesarean section
  • Change of routine practices on a patient-by-patient basis with the occurrence of complications in the surgical process
  • Presence of additional diseases
  • Emergency cases, cases using intraoperative sedation
  • Those who do not speak the language
  • Those who have an initial Mini Mental Test score lower than 24

研究组 & 干预措施

Hypotensive group

Experimental

Patients who are hypotensive (even once) and need ephedrine under spinal anesthesia with routine doses of heavy bupivacaine (Hypotension, Mean Arterial Pressure<65 mmHg, or Systolic arterial pressure < 30% will be considered an initial value.)

干预措施: Hypotension during spinal anesthesia for cesarean section (Procedure)

Hypotensive group

Experimental

Patients who are hypotensive (even once) and need ephedrine under spinal anesthesia with routine doses of heavy bupivacaine (Hypotension, Mean Arterial Pressure<65 mmHg, or Systolic arterial pressure < 30% will be considered an initial value.)

干预措施: Mini-mental test (Diagnostic Test)

Normotensive group

Placebo Comparator

Patients who are not hypotensive under spinal anesthesia with routine doses of heavy bupivacaine

干预措施: Spinal anesthesia (Procedure)

Hypotensive group

Experimental

Patients who are hypotensive (even once) and need ephedrine under spinal anesthesia with routine doses of heavy bupivacaine (Hypotension, Mean Arterial Pressure<65 mmHg, or Systolic arterial pressure < 30% will be considered an initial value.)

干预措施: Spinal anesthesia (Procedure)

Hypotensive group

Experimental

Patients who are hypotensive (even once) and need ephedrine under spinal anesthesia with routine doses of heavy bupivacaine (Hypotension, Mean Arterial Pressure<65 mmHg, or Systolic arterial pressure < 30% will be considered an initial value.)

干预措施: The Bromage scale (Diagnostic Test)

Hypotensive group

Experimental

Patients who are hypotensive (even once) and need ephedrine under spinal anesthesia with routine doses of heavy bupivacaine (Hypotension, Mean Arterial Pressure<65 mmHg, or Systolic arterial pressure < 30% will be considered an initial value.)

干预措施: Heavy Bupivacaine for spinal anesthesia (Drug)

Normotensive group

Placebo Comparator

Patients who are not hypotensive under spinal anesthesia with routine doses of heavy bupivacaine

干预措施: Mini-mental test (Diagnostic Test)

Normotensive group

Placebo Comparator

Patients who are not hypotensive under spinal anesthesia with routine doses of heavy bupivacaine

干预措施: The Bromage scale (Diagnostic Test)

Normotensive group

Placebo Comparator

Patients who are not hypotensive under spinal anesthesia with routine doses of heavy bupivacaine

干预措施: Heavy Bupivacaine for spinal anesthesia (Drug)

结局指标

主要结局

Change in postoperative cognitive function related with hypotension in cesarean section

时间窗: Preoperative (in 10 minutes before operation) to postoperative first hour.

Postoperative cognitive dysfunction is defined as the decrease in postoperative 1st hour mini-mental test results compared to preoperative results.Higher scores of mini-mental test mean a better outcome.By comparing the difference between the preoperative and postoperative mini-mental test results of the patients in the two arms, It will be observed whether there is a cognitive function difference between the groups.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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