Efficacy and Safety of Lodenafil Carbonate in the Treatment of Erectile Dysfunction in Patients With Diabetes.

Erectile Dysfunction Clinical Trial

Official title:

Efficacy and Safety of Lodenafil Carbonate in the Treatment of Erectile Dysfunction in Patient With Type II Diabetes. Multicentric Study.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01180283
• Other study ID #: CRIST 002
• Status: Completed
• Phase: Phase 4
• First received: July 29, 2010
• Last updated: August 10, 2010
• Start date: January 2009
• Est. completion date: April 2010

Study information

• Verified date: August 2010
• Source: Cristália Produtos Químicos Farmacêuticos Ltda.
• Contact: n/a
• Is FDA regulated: No
• Health authority: Brazil: Ethics CommitteeBrazil: National Health Surveillance Agency
• Study type: Interventional

Clinical Trial Summary

Sixty diabetes men with erectile dysfunction from mild to severe who agree to participate is going to have medical care approximately for 16 weeks.

During the first 4 weeks, patients will not receive any inhibitor of phosphodiesterase 5. In the following eight weeks, patients will receive oral lodenafil carbonate. They will complete the International Index of Erectile Dysfunction (IIEF) questionnaire in the site and answer the Sexual Encounter Profile (SEP) questions 2 and 3 and the Erection Hadness Score (EHS) after each intercourse or attempt without or using oral lodenafil cardonate 80mg.

Questionnaire of adverse event is included in patient diary.

Description:

This is a prospective, fixed dose, open label study.

The run in period from inclusion to conclusion will be between fourteen and sixteen weeks.

Visit zero (Vo):

• Patients will sign the informed consent form;

• Investigator will clinically evaluate the subjects regarding eligibility criteria;

• Safety laboratory tests will be perform ;

• Patients will answer the erectile function domain of the International Index of Erectile Function (IIEF);

Study coordinator:

Will orientate subjects regarding the follow:

• Patients will not use any phosphodiesterase- 5 inhibitor (iPDE-5) for four weeks;

• When intercourse or attempt happen, subjects will fill a diary;

Patients' diary includes: questions 2 and 3 of Sexual Encounter Profile (SEP), the Erectile Hardness Score (EHS) and adverse events data.

Subject will return after four weeks.

Visit One (V1):

• Patients will answer basal IIEF;

• Investigator will inform to patient the laboratory tests results;

Study coordinator:

• Will give to the patients eight pills of lodenafil carbonate;

• Will give instructions about study medication; Patient should take one pill from six to two hours before intercourse or attempt, with or without food intake or drink. The patient will not take more than one pill daily.

• When intercourse or attempt happen, subjects will fill out the diary; Patients' diary includes: questions 2 and 3 of Sexual Encounter Profile (SEP), the Erectile Hardness Score (EHS) and adverse events data.

Subject will return after four weeks.

Visit two (V2)

Study coordinator:

• Will give to patient eight pills of lodenafil carbonate;

• Will give instructions about study medication:

Patient will take one pill from six to two hours before intercourse or attempt, with or without food intake or drink. The patient will not take more than one pill daily.

• When intercourse or attempt happen, subjects will fill out the diary;

Patients' diary includes: questions 2 and 3 of Sexual Encounter Profile (SEP), the Erectile Hardness Score (EHS) and adverse events data.

Subject will return after four weeks.

Visit three (V3)

• Patients will answer the International Index of Erectile Function (IIEF);

• Safety laboratory will be perform ;

Visit four (V4)

• Investigator will inform to patients the laboratory tests results;

Complete medical evaluation including adverse event questions and physical examinations will be done at all visits.

Efficacy will be assessed by files of patients who complete the study and did not have protocol violation (per protocol population).

Main outcomes to measure efficacy: IIEF (questions 1 to 15), SEP question 2 (Were you able to insert your penis into your partner's vagina?), SEP question 3 (Did your erection last long enough for you to have successful intercourse?), EHS (Erection Hardness Score).

Tolerability will be assessed by files of patients intend to treat - subjects who took the study medication at least once.

Patients logs contain questions such as: Did you experience any uncomfortable symptoms?; At what time this symptoms began?; Did you take medication to relieve the symptoms?; Did you go to the hospital /or doctor's office?.

After review the logs, investigator will interview patients to fill adverse events reports. Investigator will assess the event intensity (from mild to severe) and will define the casual relationship to the study medication (definite; probable; possible; doubtful).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Est. completion date: April 2010
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Diabetes type II;

• Age from 18 to 65 years;

• Erectile dysfunction within the previous 6 months;

• Mild, moderate or severe erectile dysfunction by IIEF questionnaire;

• Stable sexual partner in the past 2 months;

• Preserved libido;

• Studied at least up to fourth grade;

Exclusion Criteria:

• Current beta blocker, thiazide, alpha methyldopa, antidepressants, or antiandrogen therapy intake;

• Penile prosthesis;

• Previous intolerance to sildenafil, vardenafil, tadalafil or lodenafil carbonate;

• Previous negative response to iPDE-5 correct use.;

• Penile anatomical deformities;

• Previous penile surgeries for erectile dysfunction, premature ejaculation or penile enlargement;

• Myocardial infarction or cerebral vascular accident within the previous 6 months;

• Severe or uncontrolled cardiac diseases;

• Spinal cord injury, multiple sclerosis, retinitis pigmentosa;

• Radical pelvic surgery and pelvic radiotherapy, including radical prostatectomy;

• Myocardial or Coronary Artery disease with cardiologist contraindication for using iPDE5;

• Cancer;

• Anaphylactic reactions or Steven-Johnson disease;

• Participation in another clinical trial within the last 2 months;

• Sexually transmitted diseases;

• Glycated hemoglobin > 12%;

• Testosterone < 200ng/dL;

• Prolactin > 20ng/dL;

• Hemoglobin < 10g/dL;

• Leucocytes > 14.000 cel/mm3;

• TGO > 100 U/L;

• TGP > 100 U/L;

• Creatina > 2 mg/dL;

• Investigator´s opinion;

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Erectile Dysfunction

Intervention

Drug:
• lodenafil carbonate
Dosage: lodenafil carbonate 80mg once a day. It should be taken between 6 and 2 hours before the sexual intercounter.

Locations

Country	Name	City	State
Brazil	Faculdade de Medicina do ABC	Santo André	São Paulo
Brazil	Hospital do Servidor Público Estadual de São Paulo	São Paulo	SP
Brazil	Hospital Ipiranga	São Paulo

Sponsors (1)

Lead Sponsor	Collaborator
Cristália Produtos Químicos Farmacêuticos Ltda.

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evidence that lodenafil carbonate improves erectile function in patients with diabetes type 2.	Efficacy is assessing by files of patients including questionnaires like IIEF, SEP and EHS.	16 mounths	No
Secondary	Adverse events in type 2 diabetes patients taking lodenafil carbonate and laboratory tests changes after this treatment.	Investigator will interview patients to fill adverse events reports.; Laboratory tests results before and after lodenafil carbonate treatment will be analyzed and compared, in order to detect significant changes.	16 months	Yes