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

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

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.

Study Overview

• Status: Completed
• Conditions: Erectile Dysfunction; Premature Ejaculation
• Intervention / Treatment: Other: Placebo; Other: HeezOn Ultra-1; Other: HeezOn Ultra-2

Detailed 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.

• Study Type: Interventional
• Enrollment (Actual): 15
• Phase: Not Applicable

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 26 years to 56 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Male

Description

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.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: HeezOn Ultra-1; HeezOn Ultra-1 includes ingredients like Shilajit, Galangal, Fenugreek. Dose: 2 capsules daily half an hour before dinner to be taken orally for 21 days.	Other: HeezOn Ultra-1
Active Comparator: HeezOn Ultra-2; HeezOn Ultra-2 includes ingredients like Arjuna, Galangal, Fenugreek. Dose: 2 capsules daily half an hour before dinner to be taken orally for 21 days.	Other: HeezOn Ultra-2
Placebo Comparator: Placebo; Placebo consists of Micro-crystalline Cellulose. Dose: 2 capsules daily half an hour before dinner to be taken orally for 21 days.	Other: Placebo

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Change in scores of Sexual Health Inventory for Men	Day 0, Day 1, Day 3, Day 14 and Day 28

Secondary Outcome Measures

Outcome Measure	Time Frame
Sexual Hormone Binding Globulin	Day 0 and Day 14
Free Testosterone	Day 0 and Day 14
Change in scores of Sexual Quality of Life - Male	Day 0, Day 1, Day 3, Day 14 and Day 28

Collaborators and Investigators

• Sponsor: Vedic Lifesciences Pvt. Ltd.
• Collaborators: Enovate Biolife Pvt Ltd
• Investigators: Principal Investigator: Sandip Patil, M.D., Maharashtra Medical Council; Principal Investigator: Shirish Malde, BHMS, Maharashtra Council of Homoeopathy Mumbai

Study record dates

Study Major Dates

• Study Start: May 1, 2016
• Primary Completion (Actual): January 1, 2017
• Study Completion (Actual): January 1, 2017

Study Registration Dates

• First Submitted: May 31, 2016
• First Submitted That Met QC Criteria: June 3, 2016
• First Posted (Estimate): June 9, 2016

Study Record Updates

• Last Update Posted (Estimate): January 30, 2017
• Last Update Submitted That Met QC Criteria: January 27, 2017
• Last Verified: June 1, 2016

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Mental Disorders; Sexual Dysfunctions, Psychological; Sexual Dysfunction, Physiological; Erectile Dysfunction; Premature Ejaculation
• Other Study ID Numbers: EB/151005/HZ-U/SD

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No