ClinicalTrials.Veeva

Menu

Ganglion Cell Thickness in Enuresis Nocturna

I

Izmir Bakircay University

Status

Unknown

Conditions

Enuresis, Nocturnal
Ganglion
Circadian Rhythm Disorders

Study type

Observational

Funder types

Other

Identifiers

NCT05126732
341/321

Details and patient eligibility

About

The precise role of the intrinsic circadian regulatory mechanism behind the pathogenesis of enuresis is not fully understood, but in theory, circadian rhythm irregularity may be the primary pathogenic mechanism not only for urinary outflow mechanisms but also for nocturnal bladder function. The proximity between SCN centers that control AVP release, sleep/arousal, voiding, and baroreregulation may provide the basis for circadian rhythm disturbance in one or more of these biological functions. Ganglion cells containing melanopsin pigment in the retina transmit the information they receive from the outside world about the light-dark state to the SCN via the retinohypothalamic pathway. Peripapillary retinal nerve fiber layer (RNFL) thickness, optic nerve head and macula are examined most frequently for the diagnosis of glaucoma and the detection of progression with optical coherence tomography (OCT). If differences in ganglion cell thickness can be detected using OCT in these children, a new avenue in Enuresis Nocturna may be opened.

Enrollment

50 estimated patients

Sex

All

Ages

5 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • be between the ages of 5-18
  • have enuresis

Exclusion criteria

  • have any eye conditions

Trial contacts and locations

1

Loading...

Central trial contact

Yasar ISSI

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems