Effect of OSA Resulting From Chronic Tonsillitis on Pregnancy Outcomes
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorPeking University First Hospital
About this trial
This cohort study aims to investigate the impact of obstructive sleep apnea hypopnea syndrome (OSA) resulting from chronic tonsillitis on pregnancy outcomes. The hypothesis posits that chronic tonsillitis-induced OSA may exacerbate pregnancy complications and increase the risk of adverse pregnancy outcomes.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Pregnant women confirmed with chronic tonsillitis by clinical diagnosis and presenting symptoms.
Pregnant women with a confirmed diagnosis of OSA based on polysomnography or other validated sleep monitoring techniques.
Pregnant women who are willing to participate in the study and provide informed consent.
Disqualifiers
Pregnant women with other respiratory or sleep disorders that may confound the diagnosis of OSA.
Pregnant women with severe comorbidities or medical conditions that may significantly impact pregnancy outcomes.
Pregnant women who have undergone surgical treatment for chronic tonsillitis or OSA during the study period.
Pregnant women who refuse to participate in the study or are unable to provide informed consent.
Trial population
Pregnant women who have established prenatal care records and undergone antenatal check-ups at PKUFH
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
exposure: OSA resulting from chronic tonsillitis
Other interventionexposure: OSA resulting from chronic tonsillitis
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
preterm birth rate
Time frame
10 monthsSecondary outcomes
1
delivery methods
Time frame
10 monthsOther outcomes
1
pregnancy complications
Time frame
10 months2
neonatal birth weight
birth weight of newborns measured in grams
Time frame
10 months3
neonatal length
length of newborns measured in centimeters
Time frame
10 months4
Apgar score of newborns
The Apgar score consists of five main indicators: skin color, heart rate, response to stimulation, muscle tone, and respiration. Each indicator is scored from 0 to 2, with a total score of 10. This scoring method serves as a guiding tool for the resuscitation of newborns with asphyxia and could provide a degree of predictive value for the neurological development of infants in the future.
Time frame
10 monthsLocations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: