UnknownPhase 2

Penile Intracavernosal Stem Cells Therapy for Erectile Dysfunction

Saudi Arabia30 participantsStarted 2015-10

Plain-language summary

Autologous Fat Derived Stem Cell treatment of ED. To assess safety and primary efficacy of stem cell infusion in refractory ED. To investigate the success rate and durability of success of using this new therapy in management of moderate and sever cases of erectile dysfunction.

Who can participate

Age range

40 Years – 70 Years

Sex

MALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Male 40 years old and older suffering from moderate to sever erectile dysfunction - Exclusion Criteria: * Inability to give informed consent or attend follow up * Severe diabetic neuropathy (to be defined ? Charcot joints, diabetic ulcers?) or other neuropathic disease * Viral disease from infectivity viewpoint * Major penile fibrosis or severe Peyronie's disease * Severe primary large vessel ED (defined as PSV less than 15cm/s after ICI) * Severe primary venous leakage ED (defined as EDV more than 10cm/s after ICI) * Prior systemic chemotherapy, or radiotherapy to donor or recipient area * Not in potentially active sexual relationship * Age less than 40 or over 70

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Adverse Events that occur during or after the procedure to measure safety and tolerability

Timeframe: 1 year

Trial details

NCT IDNCT02665520

SponsorElaj medical centers

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2017-03

Contact for this trial

MOHAMAD HABOUS, M.D;FEBU

+966599950131 drmhabos@hotmail.com

View on ClinicalTrials.gov More Erectile Dysfunction trials