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Efficacy of Wharton Jelly in Erectile Dysfunction

Evaluation of the Efficacy for Two Doses of Intracavernous Injection of Wharton Jelly Stem Cells for the Treatment of Diabetic Erectile Dysfunction

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03751735
Enrollment
9
Registered
2018-11-23
Start date
2017-01-27
Completion date
2019-02-26
Last updated
2019-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erectile Dysfunction Associated With Type 2 Diabetes Mellitus

Keywords

Diabetes, Wharton jelly mesenchymal stem cells, efficacy

Brief summary

Efficacy of Intracavernous injection of Wharton jelly Mesenchymal stem cells for the treatment of erectile dysfunction in diabetic patients.

Detailed description

This study will be conducted at the Cell Therapy Center (CTC), Jordan, in which 22 male patients ranging from 25-70 years diagnosed with erectile dysfunction will be selected. This diagnosis is based on medical history, validated questionnaires, physical examinations, laboratory tests and specific diagnostic tests. The patients are followed by clinical assessment, laboratory investigations as well as Doppler ultrasound. The investigators hypothesize that the intracavernous injection of stem cells will facilitate the recovery of erectile function resulting in satisfying clinical outcomes in patients.

Interventions

Intracavernous injection of Wharton Jelly Mesenchymal stem cells.

Sponsors

Sophia Al-Adwan
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
25 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Adult male patients ranging from 25 to 70 years. 2. History of chronic erectile dysfunction for at least six months. 3. Baseline international index of erectile function (IIEF) score of \< 26. 4. Not interested or able to use phosphodiesterase type 5 inhibitor (PD5i) drug therapy and willing to forgo theses treatments for the first 6 month period following study treatment. 5. Body Mass Index between 20-30. 6. Willing to provide written informed consent, complete questionnaire, and to be available for all baseline treatment and follow up examinations required by protocol.

Exclusion criteria

1. Current urinary tract or bladder infection. 2. Clinical/Laboratory evidence of transmissible diseases. 3. Clinically evident penile anatomical deformities(e.g., Peyronie's disease) or history of priapism. 4. Skin irritation, infection, wound, sore or disruption in the immediate areas of skin entry for penile injection. 5. Current or previous malignancy. 6. Use of any non study treatment for erectile function within 4 weeks of study treatment. 7. Lack of willingness to continue through 6 months after study treatment. 8. Any previous penile implant or penile vascular surgery. 9. Uncontrolled hypertension or hypotension(systolic blood pressure \> 170 or \< 90 mm Hg, and diastolic blood pressure \> 100 or \< 50 mm Hg). 10. Reported unstable cardiovascular disease (e.g., unstable angina, myocardial infarction within past 6 months, cardiac failure or life-threatening arrhythmia, congestive heart failure) or symptomatic postural hypotension within 6 months before screening. 11. Bleeding or clotting disorder, use of anticoagulant therapy. 12. Lab values for complete blood count (CBC), prothrombin time (PT)/ partial thromboplastin time (PTT)/ international normalized ratio (INR), alanine aminotransferase (ALT), aspartate aminotransferase (AST) and creatinine falling outside the normal lab values. 13. Systemic autoimmune disorder. 14. Significant active systemic or localized infection. 15. Receiving immunosuppressant medications. 16. Post-radical prostatectomy.

Design outcomes

Primary

MeasureTime frameDescription
Assessment of the efficacy of injecting Wharton Jelly derived Mesenchymal Stem Cells by Penile Doppler ultrasonography.12 monthsPatients will be evaluated for the efficacy of the intracavernous injection of Wharton Jelly derived Mesenchymal Stem Cells by Penile Doppler ultrasonography in which peak systolic velocity of the cavernosal arteries will be measured.
Assessment of the efficacy of injecting Wharton Jelly derived Mesenchymal Stem Cells by SHIM/IIEF/EHS questionnaires12 monthsThe efficacy of the intracavernous injection of Wharton Jelly will be evaluated by scoring the SHIM/IIEF/EHS questionnaires.

Countries

Jordan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026