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
Qualifiers
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 design
Treatments tested in this trial
- exposure: OSA resulting from chronic tonsillitis
Treatment groups
No treatment groups listed
Locations
Sponsors and collaborators
Source ClinicalTrials.gov