New registry aims to uncover hidden patterns of erectile dysfunction in diabetic men
NCT ID NCT07356609
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will collect information from 255 married diabetic men with erectile dysfunction (ED) in Pakistan. Researchers want to understand how common ED is, how severe it gets, and what treatments are used in real life. The goal is to improve care and guide health policies for men's sexual health.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 255 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Feb 2026
An estimate. Start dates often move.
- Expected to finish
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May 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult Male ED patients
- Ages
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18 years and older
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Adult male above 18 years of age 2. Married 3. Diabetic 4. Patient reports erectile dysfunction (symptomatic). 5. Patient is eligible to be prescribed sildenafil by treating clinician. Exclusion Criteria: 1. If at any other PDE-5 inhibitor (sildenafil, tadalafil, vardenafil, avanafil) 2. Concurrent use of organic nitrates (any form: glyceryl trinitrate, isosorbide mononitrate/dinitrate) - absolute contraindication 3. Recent or unstable cardiovascular disease * Myocardial infarction or stroke in last 3 months * Unstable angina * Uncontrolled arrhythmia or heart failure NYHA III-IV * Resting hypotension (SBP \< 90 mmHg) or uncontrolled hypertension (SBP \> 180 mmHg) per treating clinician * Known severe hepatic impairment or severe renal impairment on dialysis (if local clinician deems unsafe) * Known hypersensitivity to sildenafil or excipients * Concomitant use of potent CYP3A4 inhibitors (e.g., ritonavir) - unless clinician documents safe plan/dose adjustment
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a Patient's own blood components outperform daily ED pills?