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临床试验/RPCEC00000434
RPCEC00000434尚未招募Unknown

Exploratory, multicenter, controlled, randomized, double-blind clinical trial to evaluate the quality of life and safety of the nutritional supplement CARMINAL® in combination with conventional therapy vs. placebo in patients with ulcerative colitis in mild or moderate activity.

Catalysis Laboratories, S0 个研究点目标入组 60 人开始时间: 2024年2月29日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled trial. Masking: Double Blind. Control group: Placebo. Assignment: Parallel. Purpose: Treatment

入排标准

年龄范围
19 years 至 one(—)
性别
All

入选标准

  • 1. Patients who meet the diagnostic criteria.
  • 2. Patients aged = 19 years.
  • 3. Patients who have signed the informed consent for the research.

排除标准

  • 1. Patients with neuropsychiatric disorders that prevent the patient from expressing their willingness to participate in the study or hinder their evaluation.
  • 2. Patients with hypersensitivity or a history of allergy to Carminal® or some of its components.
  • 3. Patients with decompensated chronic diseases (diabetes mellitus, venous insufficiency, arterial hypertension, bronchial asthma, interstitial fibrosis, chronic renal failure, ischemic heart disease, symptomatic congestive heart failure, aortic stenosis, endocarditis, unstable angina pectoris, cardiac arrhythmia).
  • 4. Patient who is participating in another clinical trial or receiving another investigational product at the time of selection.

研究者

发起方
Catalysis Laboratories, S

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