Clinical Trials Directory

Trials / Completed

CompletedNCT03593720

Glans Size in Hypospadias Compared to Normal

Status
Completed
Phase
Study type
Observational
Enrollment
410 (actual)
Sponsor
Albany Medical College · Academic / Other
Sex
Male
Age
Healthy volunteers
Accepted

Summary

The investigator will collect data on penile and glans size by age, weight and ethnicity in both patients undergoing routine urological surgery and hypospadias surgery.

Detailed description

After obtaining informed consent , the investigator will measure stretched penile length and glans size in 3 dimensions (length, width, height) in the office on patients with hypospadias, as well as at the time of operation, after the induction of anesthesia. Patients undergoing hypospadias surgery will be considered study subjects. If the patient was given pre-operative testosterone as part of the current standard of care, this will be noted and the measurements taken at each pre-operative office visit will be recorded. The investigator will also record corrected age, weight in kilograms and ethnicity as identified by the family. Control patients will be those male patients undergoing non-hypospadias urological surgery (hernia repair, orchiopexy, circumcision, re-circumcision) with a normal penis, the investigator will perform a single intra-operative measurement of the same glans and penile variables after induction of anesthesia and prior to the start of their genital surgery. Again, age, weight and ethnicity will be recorded.

Conditions

Interventions

TypeNameDescription
PROCEDUREMeasurement in OfficePenile length and glans size in 3 dimensions
PROCEDUREMeasurement in ORPenile length and glans size in 3 dimensions

Timeline

Start date
2018-07-25
Primary completion
2024-12-29
Completion
2024-12-29
First posted
2018-07-20
Last updated
2025-10-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03593720. Inclusion in this directory is not an endorsement.