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Can the Hypertrophy of Contralateral Testis Predict the Absence of the Non-palpable Testis in the Boys Aged From 6months to 18months of Age ?

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02203318
Enrollment
60
Registered
2014-07-29
Start date
2014-07-31
Completion date
2015-06-30
Last updated
2016-11-01

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

Conditions

Focus of Study

Keywords

cryptorchidism, undescended testis, hypertrophy of contralateral testis

Brief summary

The aim of this study is to verify whether the hypertrophy of contralateral testis may predict the absence of the non-palpable testis in the boys younger than 24months of age. According to the previous studies of other countries, the large size of the contralateral testis of the nonpalpable testis has positive correlation woth the weak viability of the affected testis. We are going to evaluate this hypothesis with prospective study. 3 groups are going to be enrolled into this study ; non-palpable testis group(Group1), palpable but not normally descended testis group(group2) and control group(group3). The size of testis will be measured with Ultrasound and the length, width and the height will be measured before surgery at outpatient department. For the group 1 & 2, the viability of the affected testis will be evaluated and compared after surgery. In addition the comparison with normal control group is also going th be conducted.

Interventions

None listed

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
6 Months to 18 Months
Healthy volunteers
Yes

Inclusion criteria

1. neonates or Infants who visited the out-patient clinic with nonpalpable or undescended testis.(group 1, 2) aged from 6months to 18months 2. neonates or Infants aged from 6months to 18months with normal testis (volunteers, Group3)

Exclusion criteria

1. previous history of hormonal therapy. 2. chromosomal abnormality 3. previous history of abdomen or inguinal area surgery 4. children diagnosed with epididymitis or orchitis 5. twin baby 6. infants with premature (\<37 weeks) birth history

Design outcomes

Primary

MeasureTime frameDescription
Size of contralateral testis1 day of initial visitThe testicular size is measured 3-dimensionally with ultrasonography. The length, width and height will be measured and the volume of testis will be evaluated.

Countries

South Korea

Outcome results

None listed

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