A Study to Evaluate Efficacy of Investigational Product HeezOn Ultra -1/ HeezOn Ultra-2 on Male Sexual Health

Erectile Dysfunction Clinical Trial

— HeezOn-Ultra  

Official title:

A Randomized, Placebo-controlled, Double-blind Study to Evaluate Efficacy of Investigational Product HeezOn Ultra -1/ HeezOn Ultra-2 on Male Sexual Health

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02794454
• Other study ID #: EB/151005/HZ-U/SD
• Status: Completed
• Phase: N/A
• First received: May 31, 2016
• Last updated: January 27, 2017
• Start date: May 2016
• Est. completion date: January 2017

Study information

• Verified date: June 2016
• Source: Vedic Lifesciences Pvt. Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Sexual function is a part of a normal healthy life and considered to be essential for mental, physical and marital well-being. Any derangement in normal function though is a distressing situation for the individual, is often not reported due to embarrassment or due to social stigma. Sexual disorders in men are categorized according to the stage of sexual response affected in terms of disorders of erectile function, ejaculatory function or libido, albeit there is considerable potential for overlap amongst the disorders. The use of current intervention has many side-effects and has been prohibited in cardiovascular condition and also to be taken with caution with other medical condition.

This has led to the development of multiple alternate therapies which are helpful for a limited number of cases but the major concern for all these therapies is their late onset of action and not having a sustained effect.

Description:

Enovate Biolife is trying to improvise further their already marketed product HeezOn® by adding new botanicals thus naming it HeezOn Ultra. HeezOn®has been studied on 148 subjects and has proven to be beneficial for subjects with mild to moderate ED. The previous study fell short to capture the data for subjects who were also suffering from PE and their overall quality of life-related to sexual health. Therefore, the trial is designed to study the speedy and sustained effect of the improvised formula on different aspects of sexual dysfunctions.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 15
• Est. completion date: January 2017
• Est. primary completion date: January 2017
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 30 Years to 60 Years

Eligibility

Inclusion Criteria:

1. Planning to have regular sexual activity (more than twice/ week).

2. Body Mass Index should be = 29 kg/m2.

3. Subjects suffering from erectile dysfunction indicated by SHIMscore = 12 and = 16 for more than 3 months and less than 6 months.

OR

4. Subjects suffering from predominantly from premature ejaculation as indicated by PEDT score more than 11 for more than 3 months and less than 6 months.

5. Fasting blood sugar = 120 mg/dl.

6. The subjects have to be non-smoker and non-alcoholic.

Exclusion Criteria:

1. Subjects having SHIM score <12 and > 16.

2. Subjects suffering from premature ejaculation predominantly as indicated by PEDT score less than 11.

3. Subjects with major psychiatric disorders or severe systemic disorders

4. Subject having uncontrolled diabetes mellitus and hypertensive on active treatment

5. Subjects having history of male sexual dysfunction more than six months in diabetic subjects.

6. Anatomical deformity of the penis such as severe penile fibrosis or Peyronie's disease or phimosis.

7. Subjects detected with HIV and suffering from AIDS.

8. Has an abnormal thyroid stimulating hormone (TSH) level lower than 30% of lower limit normal or more than 30% of upper limit normal.

9. Has erectile dysfunction caused by neurological or endocrine factors such as hyper-prolactinemia.

10. Subjects with history of major systemic disorders.

11. Subject with history of drug abuse.

12. Subjects using medications known to cause sexual dysfunction (cimetidine, spironolactone, thiazides, adrenergic blockers, antidepressants etc.)

13. Subject has participated in any clinical trial within last 30 days.

14. Subjects not ready to sign the consent & unable to comply the protocol.

Related Conditions & MeSH terms

• Erectile Dysfunction
• Premature Ejaculation

Intervention

Other:
• HeezOn Ultra-1

• HeezOn Ultra-2

• Placebo

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
Vedic Lifesciences Pvt. Ltd.	Enovate Biolife Pvt Ltd

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in scores of Sexual Health Inventory for Men		Day 0, Day 1, Day 3, Day 14 and Day 28
Secondary	Sexual Hormone Binding Globulin		Day 0 and Day 14
Secondary	Free Testosterone		Day 0 and Day 14
Secondary	Change in scores of Sexual Quality of Life - Male		Day 0, Day 1, Day 3, Day 14 and Day 28