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CompletedNCT00990899Updated Feb 6, 2019

Hypertension and Sleep Disordered Breathing in Pediatrics

An observational study in Hypertension and Obstructive Sleep Apnea, sponsored by NYU Langone Health. Completed at 1 site in United States. Open to participants aged 10 Years to 17 Years. Per ClinicalTrials.gov, last updated 2019-02-06.

Sponsored by NYU Langone Health · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
24
Ages
10 Years to 17 Years
Sex
All
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Study summary

The primary objective is to determine the prevalence of sleep disordered breathing in children with primary hypertension or pre hypertension. The secondary objectives are to determine any association factors for children with primary hypertension or prehypertension to have sleep disordered breathing be it gender, age, body mass index (BMI), family history (hx) or ethnic group.

Read the detailed description

This is an exploratory, cross sectional study involving identification of the children of the age between 10 years and 17 years diagnosed with primary hypertension who have not been previously diagnosed and or treated for sleep disordered breathing with the revised pediatric sleep questionaire (PSQ) for sleep disordered breathing. The subjects that have shown interest will be mailed the informed consent/assent form to tbe reviewed. The consent/assent form will be handed to the child and all their questions and concerns will be answered in a comprehensible manner.

02

Conditions studied

  • Hypertension
  • Obstructive Sleep Apnea

Keywords

  • hypertension
  • obstructive sleep apnea
  • pediatrics
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In context

Sleep Apnea Syndromes

2,162 studies on the registry are indexed under Sleep Apnea Syndromes; 290 are open to participants now.

This study's enrollment of 24 is below the median of 109 across 654 observational studies indexed under Sleep Apnea Syndromes.

Browse Sleep Apnea Syndromes studies →

Lead sponsor

NYU Langone Health is the lead sponsor of 1,391 studies on the registry; 254 are open to participants now.

Of its 227 completed or terminated interventional studies of FDA-regulated products, 191 (84%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
10 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

children aged 10 to 17 years who have been diagnosed with primary hypertension

Inclusion criteria

  • aged 10 to 17 years old diagnosed with primary hypertension

Exclusion criteria

Exclusion Criteria:

  • refused to participate in the study
  • children to secondary hypertension
  • previously diagnosed with sleep disordered breathing
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Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
24 participants (actual)
06

Study locations

1 site
  • Winthrop University Hospital
    Mineola, New York 11501, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 6, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00990899
Lead sponsor
NYU Langone Health
Responsible party
Sponsor
First posted
Oct 7, 2009
Start date
Oct 2008
Primary completion
Jul 2011
Completion
Jul 2011
Last update
Feb 6, 2019

Study contacts

Melodi Pirzada, MD
principal investigator · Winthrop University Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2019. You cannot join it, but the record below documents what was studied.

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