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临床试验/DRKS00031624
DRKS00031624尚未招募不适用

Evaluation of therapeutic response of chronic inflammatory bowel diseases by deep morphological phenotyping - „PicIBD (Picture IBD)

KSH Kiel0 个研究点目标入组 400 人开始时间: 2024年2月20日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
400

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Active inflammatory bowel disease
  • -Indication for biological therapy (independent of recruitment for study)
  • -written informed consent
  • -stable dosage of corticosteroids (prednisone =20mg/day for at least 2 weeks or <20mg/day for at least 40 days)
  • -stable dosages of immunomodulators (=1.5mg/kg/day or the highest tolerated dosage of azathioprine or =1 mg/kg/day or the highest tolerated dosage of 6-mercaptopurine with stable dosage for =1 month prior to baseline) for 1 month
  • -stable dosage of rectal therapies with mesalamine or glucocorticoids is necessary at least two weeks before index examination.

排除标准

  • -missing consent of the patient
  • -known or suspected hypersensitivity to contrast agent fluorescein and/or butylscopolamin
  • -gastrointestinal obstruction or suspected perforation
  • -serious cardiovascular, renal or hepatic disease
  • -impaired coagulation
  • -elevated serum creatinine
  • -acute diverticulitis
  • -concomitant viral colitis i.e. cytomegalovirus infection
  • -NSAID use and use of any medication that could potentially cause or aggravate colitis during the last four weeks prior initiation of biological therapy
  • -toxic megacolon
  • -abdominal abscess
  • -increased risk of infectious complications
  • (e.g. pyogenic infection <4weeks, enteric pathogens detected on stool analysis, active or latent tuberculosis, immunodeficiency, hepatitis B or C, live vaccination <4weeks),
  • -pregnancy or lactation
  • -malignant neoplasms

研究者

发起方
KSH Kiel

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