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临床试验/NCT05848531
NCT05848531招募中4 期

Advantage of Clonidine With Morphine In Patient Controlled Analgesia Pump for the Treatment of Vaso-occlusive Crisis in Sickle Cell Disease Patients

Centre Hospitalier Universitaire Saint Pierre1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年4月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
40
试验地点
1
主要终点
Morphine Consumption

研究概览

简要总结

Vaso-occlusive crisis are highly painful in Sickle-cell patients. Morphine is the treatment of choice for this pain. Various adjuncts have been studied for the treatment of vaso-occlusive crisis.

The investigators aimed to study the effect of clonidine associated with morphine in PCIA (patient controlled intravenous analgesia pumps) regimen. The investigators will compare it to the morphine alone in PCIA for the treatment of vaso-occlusive pain.

The investigators will measure the morphine consumption of all patient, the impact on the apparition of the morphine secondary effect and on inflammation biomarkers and the biopsychosocial respond.

Each patient will be hospitalized and follow by haematologist from the hospital, pain doctors and nurses.

It will be a double blind randomised, prospective study. The randomisation will be done by the pharmacy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

盲法说明

Unmarked bags of products, randomised before administration.

入排标准

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

入选标准

  • Vaso-Occlusive Crisis In Sickle Cell disease Patients

排除标准

  • Patient's refusal
  • Pregnancy
  • Contr-indication Clonidine therapy

研究组 & 干预措施

Clonidine and Morphine

Experimental

Morphine Associated with Clonidine PCIA

干预措施: Clonidine (Drug)

结局指标

主要结局

Morphine Consumption

时间窗: Up to two weeks

Morphine Consumption during hospitalisation

次要结局

  • Numerical Rating Scale(Up to two weeks)
  • Biology markers(Up to two weeks)
  • Biopsychosocial model / ASCQ-ME questionary(Up to two weeks)

研究者

发起方
Centre Hospitalier Universitaire Saint Pierre
申办方类型
Other
责任方
Principal Investigator
主要研究者

Lara Chow Yuen

Principal Investigator

Centre Hospitalier Universitaire Saint Pierre

研究点 (1)

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