Trial | NCT02152579  Report issue

Title

Efficacy and Safety of Monocordil Manufactured by Laboratórios Baldacci
Open Monocentric Clinical Study for the Evaluation of Efficacy and Safety of 20 mg Monocordil Tablets Manufactured by Laboratórios Baldacci in Patients With Stable Angina

  • Phase

    Phase 3

  • Study Type

    Interventional

  • Status

    Unknown status

  • Intervention/Treatment

    isosorbide ...

  • Study Participants

    86
Phase III clinical study for the evaluation of clinic and cardiologic effects of isosorbide mononitrate from the incidence of events (angina episodes).

This is an open, comparative, monocentric trial. The hypothesis, regarding the number of angina episodes, to be tested are:

H0: μD = 0 ot H0: μAfter = μBefore
HA: μD ≠ 0 ot HA: μBefore ≠ μAfter
Phase III study, monocentric, open, with a single treatment arm in patients with stable angina to evaluates efficacy and safety. The study will be sponsored by pelo Laboratórios Baldacci. All patients who participate in the study shall sign two copies of the informed consent form. The inclusion of patients is expected to last until 12 months from the approval of the Ethics Committee and ANVISA.

Follow up will last at least 2 weeks for each included patient. A total of 86 patients will be recruited for this study and all of them will initiate treatment with 20 mg monocordil tablets. After 2 consecutive weeks using the investigational product (+2 days), the patients will be evaluated again, particularly for the parameters under study, this is, quantity and severity of angina episodes and adverse events. The selected patients shall also be 18-80 years old of both genders, with proved diagnosis of stable angina through clinical exams such as ECG, physical effort tests or similar. Patients will receive 20mg monocordil tablets (Baldacci Laboratories).

The evaluations will take place in two opportunities: one at the visit of medical evaluation and recruitment in the study (along with the deliver of the study medication and a diary) and the second one after 2 weeks (+2 days) of use of 20mg monocordil tablets for medical evaluation and discharge of the study (return of the diary and medication accountability).
Study Started
Jul 31
2014
Primary Completion
Sep 30
2014
Anticipated
Study Completion
Oct 31
2014
Anticipated
Last Update
Jun 02
2014
Estimate

Drug Isosorbide-5-mononitrate

Patients will receive 20mg monocordil tablets (Baldacci Laboratories).

  • Other names: Monocordil

Isosorbide-5-mononitrate, tablet Experimental

Single treatment arm.

Criteria 

Inclusion Criteria:

Capacity for understanding and agreement in signing the informed consent form
Age 18 between 18 and 80 years old
Have a diagnosis of stable angina, proved by ECG, test of physical effort or similar
Not being under treatment with other nitrate for stable angina
Medical indication for the use of isosorbide mononitrate (Monocordil)

Exclusion Criteria:

Presence or serious comorbidities (under judgement of the investigator)
Allergy to any of the component of the investigational product
Pregnant female patients, brest feeding and/or in fertile condition who wish to get pregnant during the study and deny the use of contraceptives
No Results Posted