跳至主要内容
临床试验/CTRI/2014/08/004841
CTRI/2014/08/004841招募中未知

An Open Label, Single Center Study to assess the effect of IminoNorm on the Glycaemic index of common carbohydrates

Phynova Group0 个研究点目标入组 12 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Healthy Volunteers with a BMI between 18 and 25
  • Non-Diabetic or any pre-diabetic conditions demonstrated by a fasting blood sugar between 3.9 to 5.5 mmols/L (70 - 100mg/dL).Not on any diabetic or insulin resistance medication

排除标准

  • Abnormal laboratory values at screening.
  • Pregnant or Lactating women
  • Subjects with any cardio-vascular diseases
  • Subjects otherwise judged by the PI not fit to participate in the study
  • Any past significant medical history
  • Any Psychiatric disorder or on any such medications
  • Any malignancy or history of malignancies
  • Any known hypersensitivity or allergy
  • Recent participation (within the last 3 months) in any other clinical trial

研究者

发起方
Phynova Group

相似试验

进行中(未招募)
不适用
An open-label, multicenter study to evaluate the efficacy and tolerability of a 4 week therapy with the combination of valsartan 160 mg plus amlodipine 5 mg in hypertensive patients not adequately responding to a 4 week treatment with amlodipine 5 mg or felodipine 5 mg in monotherapy - ExPress - Mmoderate essential hypertensionMedDRA version: M15Level: LLTClassification code 10015488
EUCTR2006-001484-39-DEovartis Pharma GmbH230
进行中(未招募)
不适用
An open-label, multicenter study to evaluate the efficacy and tolerability of a 4 week therapy with the fixed dose combination of valsartan 160 mg plus HCTZ 25 mg in hypertensive patients not adequately responding to a 4 week therapy with the free combination of an angiotensin receptor blocker (candersartan 32 mg) plus HCTZ 25 mg - CICERO
EUCTR2006-001311-30-DEovartis Pharma GmbH220
进行中(未招募)
1 期
A study to to evaluate the efficacy, safety and tolerability of PDNO (nitrosooxypropanol) infusion in COVID-19 patients with high blood pressure in lung arteries.Acute pulmonary hypertension during COVID-19 infectionMedDRA version: 20.0Level: HLTClassification code 10037401Term: Pulmonary hypertensionsSystem Organ Class: 100000004855
EUCTR2020-002982-33-SEAttgeno AB16
进行中(未招募)
不适用
An open-label, multicenter study to evaluate the efficacy and safety of a 5 week therapy with the combination of valsartan 160 mg plus amlodipine 10 mg in hypertensive patients not adequately responding to a 5 week therapy with ramipril 5 mg and felodipine 5 mgPatients with essential hypertensionMedDRA version: M15Level: LLTClassification code 10015488
EUCTR2005-003976-39-DEovartis Pharma GmbH200
进行中(未招募)
不适用
An open-label, multicenter study to evaluate the efficacy and safety of a 4 week therapy with the single pill (SPC) combination of Aliskiren 300 mg / Amlodipine 10 mg in hypertensive patients not adequately respond to an uptitrated 4 week therapy with the SPC of Olmesartan 40 mg / Amlodipine 10 mg, with a potential extention if patients still not adequately respond with a 4 week therapy with the SPC Aliskiren 300 mg / Amlodipine 10 mg / HCTZ 12,5 mg - AWESOMEessential hypertensionMedDRA version: 12.1Level: LLTClassification code 10015488Term: Essential hypertension
EUCTR2009-016693-33-DEovartis Pharma GmbH