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临床试验/NCT05053763
NCT05053763Unknown不适用

The 90% Effective Dose of Remimazolam for Duodenoscopy Insertion During ERCP

Jianbo Yu1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2021年9月22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
发起方
入组人数
120
试验地点
1
主要终点
The number of success duodenoscopy insertion

研究概览

简要总结

Remimazolam has shown promising results for sedation in colonoscopy . Alfentanil is widely used in the analgesia of ERCP . The purpose of the study was to determine the 90% Effective Dose of Remimazolam for Duodenoscopy Insertion During ERCP With Alfentanil 10µg/kg

详细描述

  1. Title:The 90% Effective Dose of Remimazolam for Duodenoscopy Insertion During ERCP With Alfentanil 10µg/kg 2. Research center: Single center. 3. The population of the study: Age is between 18 and 85 years; ASA I-III levels; Patients undergone elective ERCP surgery, non-intubation patients; 4. Sample size:The sample size was decided based on that of prior Literature.The study was carried out using a biased coin design up-and-down sequential method, where the dose of remimazolam administered to each patient depended on the response of the previous one with success/failure duodenoscopy insertion during ERCP are required for reliable estimates. The first patient recruited received a dose of 0.2mg/kg, based on our past experience.Subsequently, if a patient had a failure duodenoscopy insertion, the dose of remimazolam was increased by 0.025mg/kg in the next subject. If a patient had a successful duodenoscopy insertion the next subject was randomised to receive either a lower dose (with a decrement of 0.025mg/kg), with a probability of b = 0.11, or the same dose, with a probability of 1-b = 0.89.

We defined duodenoscopy insertion a failure was as gross purposeful muscular movement, coughing or vomiting occurring during or within 2 minutes of insertion of duodenoscopy. If BIS>75 and MOAA/S > 1 when 3 min after the intravenous injection of remimazolam, it was considered a failure, and the patient received rescue sedation. Success was depicted when the reactions mentioned earlier were absent.

研究设计

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

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age is between 18 and 85 years
  • ASA I-III levels;
  • Patients undergone elective ERCP surgery, non-intubation patients;

排除标准

  • Chronic pain with long-term use of analgesics, psychotropic substances (including opioids, NSAIDs, sedatives, antidepressants), alcohol abusers, with known drug allergy;
  • BMI<18 or BMI>30;
  • Previous abnormal surgical anesthesia recovery history;
  • Hypertension or systolic blood pressure greater than 160 mmHg or diastolic blood pressure greater than 95 mmHg when the patient admission to the operating room
  • Suffering from esophageal reflux; • Sedatives, analgesics and antipruritic drugs were used 24 hours before operation;
  • Expected difficult intubation ;
  • Opioids allergy history;
  • Take monoamine oxidase inhibitor or antidepressant within 15 days;
  • Pregnant or parturient women;
  • Involved in other drug trials within three months;
  • Patients who can not communicate well with the researcher

研究组 & 干预措施

Experimental: age<65 group

Other

The 90% effective dose of remimazolam for duodenoscopy insertion with alfentanil 10µg/kg

干预措施: Remimazolam (Drug)

Active Comparator:age ≥65 group

Other

The 90% effective dose of remimazolam for duodenoscopy insertion with alfentanil 10µg/kg

干预措施: Remimazolam (Drug)

结局指标

主要结局

The number of success duodenoscopy insertion

时间窗: 1 day

success duodenoscopy insertion is defined by no body movement

次要结局

  • The number of the occurrence of bradycardia(1 day)
  • The number of the occurrence of hypotension(1 day)
  • The number of the occurrence of injection pain(1 day)

研究者

发起方
Jianbo Yu
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jianbo Yu

Director

Tianjin Nankai Hospital

研究点 (1)

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