Trial · NCT07902362
Investigation of Serum Sclerostin Levels in Patients With Erectile Dysfunction
NCT07902362, Completed, Medipol University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Investigation of Serum Sclerostin Levels in Patients With Erectile Dysfunction. Trials, record NCT07902362. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07902362
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Investigation of Serum Sclerostin Levels in Patients With Erectile Dysfunction
- NCT number
- NCT07902362
- Status
- Completed
- Enrollment
- 97 participants, actual
- Lead sponsor
- Medipol University
- Conditions
- Erectile Dysfunction
- First posted
- 2026-10-28
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Peripheral Serum Sclerostin Levels | Baseline | The primary outcome is the difference in peripheral venous serum sclerostin levels between patients with erectile dysfunction and healthy controls, measured via the Enzyme-Linked ImmunoSorbent Assay (ELISA) method in ng/ml. |
| Secondary | Cavernosal Serum Sclerostin Levels | Baseline (15 minutes post-injection) | Cavernosal blood serum sclerostin levels evaluated exclusively in the erectile dysfunction group following the Combined Intracavernosal Injection and Stimulation Test, measured via ELISA in ng/ml. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers7
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07902362
GET https://conductscience.org/api/trials/v1/NCT07902362/registered