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临床试验/NCT03126045
NCT03126045已完成不适用

SPPLAASH Study : a Randomized Study Aiming at Evaluating the Incidence of Post Lumbar Puncture Headache (PLPH) With the Use of Atraumatic Needles in Hematology

Centre Hospitalier Universitaire de Saint Etienne4 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2017年8月22日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
68
试验地点
4
主要终点
Number of headache

研究概览

简要总结

Lumbar punctures are implemented for the diagnosis of patients with hematologic symptoms as well as for the intrathecal chemotherapy injections. Post lumbar puncture headache is a common complication for patients and is characterized by the occurrence of a headache with an orthostatic component, with additional symptoms such as nausea. Some studies in neurology, anesthesia and gynecology have previously shown a decreased incidence for post lumbar puncture headache while using atraumatic needles as compared to standard needles. In this context, it is necessary to better document the incidence of post lumbar puncture headache with the use of atraumatic needles in hematologic patients.

详细描述

Lumbar punctures (LP) are implemented for the diagnosis of patients with hematologic symptoms as well as for the intrathecal chemotherapy injections. Post lumbar puncture headache (PLPH) is a common complication in around 30% of patients. PLPH is characterized by the occurrence of a headache with an orthostatic component within 12-72 hours after LP with additional symptoms such as nausea. Even if this phenomenon spontaneously resolves within 3 to 5 days, symptoms can immobilize the patient and can interfere with his daily activities. Technical procedures largely influence the incidence of PLPH. Indeed, some studies in neurology, anesthesia and gynecology have previously shown a decreased incidence for PLHP while using atraumatic needles as compared to standard needles. So far, few data are available for hematology. In this context, it is necessary to better document the incidence of PLPH with the use of atraumatic needles in hematologic patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Outcomes Assessor)

盲法说明

Neither patients know the needle used during the spinal punction, nor the person collecting the information.

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

  • Patients with hematologic syndromes undergoing a diagnostic lumbar puncture
  • Signed written informed consent form
  • Patient affiliated to a social security regimen or beneficiary of the same

排除标准

  • Any known contraindication for the lumbar puncture procedure: increased intracranial pressure, blood clotting disorder, thrombocytopenia
  • Any known infection
  • Patient with a Body Mass index < 18 or Body Mass index > 40
  • Any patient that requires an ultrasound guided lumbar puncture
  • Patient that underwent a lumbar puncture within 6 months
  • Patient under guardianship or deprived of his liberty or any condition that may affect the patient's ability to understand and sign the informed consent (art. L.1121-6, L.112-7, L.1211-8, L.1211-9)
  • Refusing participation
  • Pregnancy or breastfeeding women

结局指标

主要结局

Number of headache

时间窗: 5 days

Incidence of patients with mild and severe headache within 5 days following lumbar puncture as evaluated by verbal rating scales (intensity score ≥4) will be reported.

次要结局

  • Intensity of headache(5 days)
  • Duration of significant headache(5 days)
  • Pain intensity(5 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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