Study to Evaluate the Efficacy and Tolerability of Apevinat BC Compared to Vitamin Complex

The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2011 by MDCPharma Produtos Farmaceuticos LTDA.
Recruitment status was  Not yet recruiting
Sponsor:
Information provided by:
MDCPharma Produtos Farmaceuticos LTDA
ClinicalTrials.gov Identifier:
NCT01295450
First received: January 19, 2011
Last updated: February 11, 2011
Last verified: February 2011

January 19, 2011
February 11, 2011
April 2011
August 2011   (final data collection date for primary outcome measure)
Evaluate the effectiveness of Apevinat BC in appetite stimulation. [ Time Frame: 30 days ] [ Designated as safety issue: Yes ]
Evaluate the efficacy of BC Apevinat in appetite stimulation compared to vitamins.
Same as current
Complete list of historical versions of study NCT01295450 on ClinicalTrials.gov Archive Site
Evaluate the tolerability of Apevinat BC in appetite stimulation. [ Time Frame: 30 days ] [ Designated as safety issue: Yes ]
To evaluate the tolerability of Apevinat BC in appetite stimulation compared to vitamins.
Same as current
Not Provided
Not Provided
 
Study to Evaluate the Efficacy and Tolerability of Apevinat BC Compared to Vitamin Complex
A Clinical Multicenter, Phase III, Randomized, Double-blind, Prospectively to Evaluate the Efficacy and Tolerability of Apevinat BC Compared to Vitamin Complex in Stimulating the Appetite

The purpose of this study is to evaluate the efficacy and tolerability of Apevinat BC compared to vitamin complex, in the treatment of lack of appetite and prevention of deficiency of B and C vitamins.

Apevinat BC presents in its formula the cyproheptadine hydrochloride, which is an antihistamine and anti-serotonin with stimulant of appetite property associated with the vitamin B complex and C, in balanced amounts.

This combination is specially formulated to adequately serve patients with anorexia represented by lack of appetite or appetite diverted to diets without the necessary vitamins. For the anorexic patients that are common B and C hypovitaminosis, the use of Apevinat BC will have a synergistic and joint action to increase appetite and facilitate correction of a diet while also supplement with B and C vitamins, this association does not decreases its tolerability and safety but hits adequately the purpose of therapeutic orexigenic.

The current study will compare the efficacy and tolerability of Apevinat BC to vitamin complex administered three times a day, in the prevention and treatment of lack of appetite and B and C hypovitaminosis.

Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
  • Lack of Appetite
  • Anorexia
  • Drug: Apevinat BC

    Apevinat BC presents in its formula the cyproheptadine hydrochloride (0,800 mg), tiamin hydrochloride(0,120 mg), Riboflavin sodium phosphate (0,200 mg), nicotinamide (1,334 mg, piridoxin hydrochloride (0,134 mg), ascorbic acid (4,334 mg).

    Administer the recommended dosage for children 7 to 14, preferably one hour before meals: 5 ml three times daily.

    Other Names:
    • Apevinat BC
    • MDCPharma
  • Drug: Vitamin Complex
    A vitamin complex contains: B1, B2, B3, B3 and C vitamins. Administer the recommended dosage preferably one hour before meals: 5 ml three times daily.
    Other Name: Polivitamin, B and C Complex.
  • Active Comparator: Vitamin Complex
    A vitamin complex contains: B1, B2, B3, B3 and C vitamins. Administer the recommended dosage preferably one hour before meals: 5 ml three times daily.
    Intervention: Drug: Apevinat BC
  • Experimental: Apevinat BC

    Apevinat BC presents in its formula the cyproheptadine hydrochloride (0,800 mg), tiamin hydrochloride(0,120 mg), Riboflavin sodium phosphate (0,200 mg), nicotinamide (1,334 mg, piridoxin hydrochloride (0,134 mg), ascorbic acid (4,334 mg).

    Administer the recommended dosage for children 7 to 14, preferably one hour before meals: 5 ml three times daily.

    Intervention: Drug: Vitamin Complex
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Not yet recruiting
74
August 2011
August 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients who presents lack of appetite;
  • Wash out 20 days after ingestion before similar drug;
  • Responsible for the least able to understand and maintain their adherence to protocol;
  • Patients of all ethnic groups of both sexes, aged 7-14 years;
  • Responsible for the minor must consent to participate in the same study, through the signing of consentiment term;
  • Responsible for the minor should be able to understand the proper use of medication;

Exclusion Criteria:

  • Patients with parasitic infections;
  • Patients with angle closure glaucoma or open;
  • Patients with a predisposition to urinary retention;
  • Patients with peptic ulcer or stenotic pylorus-duodenal obstruction;
  • debilitated patients or in acute asthma attack;
  • Patients who have poor appetite caused by any serious illness;
  • Patients who are taking any medications that depress the central nervous system;
  • Patients who take medication monoamine oxidase inhibitors, tricyclic antidepressants, phenothiazine, probenecid, levodopa, phenytoin, phenobarbital, chloramphenicol, cyclophosphamide, cyclosporine, chlorambucil, corticotrophin, mercaptopurine, isoniazid, penicillin, estrogens, contraceptives, haloperidol, ipatrópico, barbiturates, Primidone, salicylates;
  • Patients with known hypersensitivity to any components of the formula;
  • Patients who are participating in another clinical trial;
  • Inability to compliance with the protocol;
  • Any condition that in the opinion of the investigator would prohibit the inclusion and patient compliance with the protocol.
Both
7 Years to 14 Years
No
Contact: Anete S Grumach, Investigator 55 (11) 4993-5468 grumach@usp.br
Contact: Adriana P Albuquerque, Coordenator 55 (11) 4438-3558 adrianaalbuquerque@fmabc.br
Brazil
 
NCT01295450
MDC-APEVINAT-01/10
Yes
MDCPharma Produtos Farmaceuticos LTDA, Industry
MDCPharma Produtos Farmaceuticos LTDA
Not Provided
Principal Investigator: Joaquim CS D' Azevedo, Investigator A/Z Clinical
Principal Investigator: Felicio S Neto, Investigator Dr. Felicio Savioli Clinical
MDCPharma Produtos Farmaceuticos LTDA
February 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP