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临床试验/NCT01086865
NCT01086865Unknown3 期

Clinical Study Phase III, Randomized, Double-blind, Prospective and Comparative to Evaluate the Efficacy and Tolerability of Using APETIVITON BC Compared to Petivit BC in Appetite Stimulate.

Cifarma Cientifica Farmaceutica Ltda0 个研究点目标入组 150 人开始时间: 2010年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
入组人数
150
主要终点
Evaluate the effectiveness of apetiviton BC compared to Petivit BC in appetite stimulation in children, adults and seniors.

研究概览

简要总结

Clinical study phase III, randomized, double-blind, prospective, comparative non-inferiority to evaluate the efficacy and tolerability of using APETIVITON BC compared to Petivit BC in appetite stimulate in children, adults and elderly.

详细描述

Clinical trial phase III, randomized, double-blind, prospective, comparative non-inferiority to evaluate the efficacy and tolerability of using APETIVITON BC compared to Petivit BC stimulation of appetite in children, adults and elderly. A total of 150 patients, distributed as follows:

25 patients treated children Apetiviton BC,25 patients treated children Petivit BC, (2-6 years).

25 adult patients treated with Apetiviton BC,25 adult patients treated with Petivit BC, (18-50 years.

25 elderly patients treated with Apetiviton BC,25 elderly patients treated with Petivit BC. (60-80 years.

研究设计

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

入排标准

年龄范围
2 Years 至 80 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • For both groups:
  • Patients who have inappetence;
  • Patients able to understand and maintain adherence to protocol;
  • Wash-out 20 days after ingestion of prior similar drug;
  • Patients able to understand the correct use of medication;
  • Patients who consent to participate in the study by signing the inform consent;
  • Patients of any ethnic group male and female, aged between 2 and 6 years;
  • Patients of any ethnic group male and female, aged between 18 and 50 years;
  • Female patients in childbearing age, sexually active, make pregnancy test result should be negative and, furthermore, should be using contraceptive methods such as contraception, condom, IUD and diaphragm.
  • Patients of any ethnic group male and female, aged between 60 and 80 years.
  • Female patients in childbearing age, sexually active, make pregnancy test result should be negative and, furthermore, should be using contraceptive methods such as contraception, condom, IUD and diaphragm.

排除标准

  • For both groups:
  • Patients with glaucoma open or closure angle;
  • Patients with predisposition to urinary retention;
  • Patients with stenous peptic ulcer or pylorus-duodenal obstruction;
  • Debilitated patients or in acute attack of asthma;
  • Alcoholic;
  • Patients who have loss of appetite caused by any serious disease;
  • Patients who make use of any drugs central nervous system depressants;
  • Patients who make use of medicines monoaminooxidase inhibitors, tricyclic antidepressants, phenothiazines, probenecid, levodopa, phenytoin, phenobarbital, chloramphenicol, cyclophosphamide, cyclosporine, chlorambucil, corticotropin, mercaptopurine, isoniazid, penicillin, estrogens, contraceptives, haloperidol, ipatrópico, barbiturates, primidone, salicylates;
  • Patients with known hypersensitivity to any components of the formula;
  • Patient who is participating in another clinical study;
  • No able to adhere to protocol;
  • Patients who are pregnant or breastfeeding;
  • Any condition that in the opinion of the investigator can impossible to include the patient's adherence to the protocol.

研究组 & 干预措施

Petivit BC

Active Comparator

干预措施: Apetiviton BC (Drug)

Apetiviton BC

Experimental

干预措施: Apetiviton BC (Drug)

结局指标

主要结局

Evaluate the effectiveness of apetiviton BC compared to Petivit BC in appetite stimulation in children, adults and seniors.

时间窗: 30 days

次要结局

  • Evaluate the tolerability of apetiviton BC compared to Petivit BC the stimulation of appetite in children, adults and seniors(30 days)

研究者

申办方类型
Industry

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