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Could your own belly fat fix ED after prostate cancer surgery?

NCT ID NCT07355530

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether a single injection of a patient's own fat-derived stem cells into the penis could improve erectile dysfunction after prostate removal. 70 men who had poor erections for over a year after surgery were enrolled. Half received the stem cell injection, half got a placebo. All had liposuction to harvest the cells. Researchers measured changes in erectile function using questionnaires over 12 months.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Adipose-derived regenerative cells (stem cells from the patient's own fat)
What this could lead to
If it works, this could offer a new, one-time treatment for erectile dysfunction after prostate surgery, reducing the need for daily medication.
What could go wrong
This is a small, early-phase trial with only 70 participants. The treatment may not work better than placebo, and the effects may not last. All patients had liposuction, which carries its own risks.

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.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

70 people

The number who actually took part.

Started

Jan 2018

Finished

Mar 2021

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Male participants only

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion criteria: * Nervesparing robot assisted RP * Erectile dysfunction for more than a year after RP * Normal erectile function before RP (IIEF-5 \> 22) and postoperative IIEF-5 score 5-20 or EHS 1 * Involved in a monogamous, heterosexual relationship (since questionnaires are only valid for heterosexual relationsships), where both parts are interested in sexual activities * Insufficient effect of standard medical treatment for ED * Subcutaneous adipose deposits on the abdomen \> 120 mL * Performance status 0 * Ability to give informed consent * Proficiency in the Danish language to understand the questionnaires IIEF-5 and EHS Exclusion criteria: * Problems with general anesthesia * Incontinence after RP * Anti-thrombotic treatment that cannot be discontinued or substituted with heparin * No interest in sexual interaction with a partner * Previous pelvic surgery or radiation * Systemic autoimmune disease * Alcohol or drug abuse

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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.

Contacts and locations

Locations

  • Odense Universityhospital

    Odense, 5000, Denmark

More trials for these conditions

Other studies related to the condition(s) this trial covers.