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临床试验/ISRCTN12678718
ISRCTN12678718已完成未知

The acute and chronic effects of gut neuropeptides on intracranial pressure regulation

niversity of Birmingham0 个研究点目标入组 15 人开始时间: 2017年7月18日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
15

研究概览

简要总结

2022 Other publications in https://pubmed.ncbi.nlm.nih.gov/36320018/ Evaluation of telemetric intracranial pressure monitoring (added 03/11/2022) 2022 Preprint results in https://doi.org/10.1101/2022.05.24.22275518 Exenatide results (added 07/11/2022) 2022 Abstract results in https://doi.org/10.1186/s10194-022-01527-4 (added 05/08/2024) 2020 Other publications in https://pubmed.ncbi.nlm.nih.gov/33090189/ (added 05/08/2024) 2023 Other publications in https://pubmed.ncbi.nlm.nih.gov/38487358/ Sub-study (added 05/08/2024)

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 2. Aged 18-60 years old
  • 3. Diagnosed with IIH by the modified Dandy criteria
  • 4. Active disease (papilloedema Frisen grade greater than 1)
  • 5. Significantly raised ICP (greater than 25cm CSF)
  • 6. No evidence of venous sinus thrombosis (documented normal MR Venogram of CT Venogram)
  • 6. Able to provide informed consent

排除标准

  • 1. Aged less than 18 or older than 60 years
  • 2. Pregnant or trying to conceive
  • 3. Significant co-morbidity, such that in the opinion of the investigator it would not be in the participant’s best interest to participate in the trial
  • 4. Addison’s or Cushing’s disease
  • 5. Functioning CSF shunt/stent or optic nerve sheath fenestration
  • 6. Currently using GLP-1 agonist or DPP-4 inhibitor
  • 7. Surgical contra-indication
  • 8. Concomitant therapy with acetazolomide, topiramate or diuretics (this can be discontinued 1 month prior to enrolment)
  • 9. Inability to give informed consent e.g. due to cognitive impairment

研究者

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