Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00462306 · ClinicalTrials.gov registry record
Incidence of Obstructive Sleep Apnea in Pregnancy
A clinical trial, sponsored by Northwestern University.
- Completed
- Registry status
- 4,577
- Enrollment target
NCT00462306: Completed study, sponsored by Northwestern University.
NCT00462306 is a clinical trial that has completed, run by Northwestern University. The registered enrollment target is 4,577 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00462306 has completed, sponsored by Northwestern University.
- COMPLETED
- Registry status
- 4,577 participants
- Enrollment target
Study Summary
Obstructive sleep apnea is a condition characterized by obstruction of the upper airways and episodes of apnea and hypopnea during sleep. It is associated with significant adverse health effects. The incidence of obstructive sleep apnea in the general female population is approximately 2% but the incidence of obstructive sleep apnea in pregnancy is unknown. There is some evidence that pregnancy precipitates or at least exacerbates this condition and that there may be a relationship between intrauterine fetal growth retardation and maternal preeclampsia. In addition, there are several anesthetic implications that are concern for the patient with obstructive sleep apnea. These include: exquisite sensitivity to all central nervous system depressant drugs and the potential for upper airway obstruction or apnea with even minimal drug doses; difficult mask ventilation; difficult intubation; arterial hypoxemia; arterial hypercarbia; polycythemia; hypertension; pulmonary hypertension and cardiac failure. All of these conditions pose significant anesthetic risk for the patient, and this risk may be increased further by pregnancy.
Primary Outcome
The Berlin Questionnaire consists of three categories designed to elicit information regarding snoring (category 1), daytime somnolence (category 2), and the presence of obesity and/or hypertension (category 3). Categories 1 and 2 are considered positive if 2 or more responses are positive category 3 is considered positive if 1 response is positive and/or the body mass index is greater than 30 kg per meter squared. A patient is considered to have a high likelihood of sleep disordered breathing i
Interventions
- PROCEDURE Survey: Berlin questionnaire
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 4,577 participants |
| Start Date | 2005-09 |
| Est. Completion | 2008-06 |
What the finished NCT00462306 record still lists
NCT00462306 is an observational study that tracks outcomes without assigning an intervention. Its 4,577 participants enrollment target places it among the larger protocols in the corpus.
The record links to 0 conditions, and to 1 intervention - of which Survey: Berlin questionnaire is the first listed.
NCT00462306 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00462306 about?
NCT00462306 is a clinical study titled "Incidence of Obstructive Sleep Apnea in Pregnancy". Obstructive sleep apnea is a condition characterized by obstruction of the upper airways and episodes of apnea and hypopnea during sleep. It is associated with significant adverse health effects. The incidence of obstructive sleep apnea in the general female population is approximately 2% but the in...
What is the current status of trial NCT00462306?
This trial is currently completed. The enrollment target is 4,577 participants. The study started on 2005-09. Estimated completion is 2008-06.
What interventions are being tested in trial NCT00462306?
The interventions under investigation include: Survey: Berlin questionnaire (PROCEDURE).
Who is sponsoring clinical trial NCT00462306?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT05768217 · 4,600 participants · NA
Community Resiliency Collective Efficacy Intervention
- NCT06535139 · 4,630 participants · NA
ReMARK: Addressing Disparities in Rural HPV-related Cancer Prevention
- NCT06702878 · 4,514 participants · Phase 3
Light-Activated Antimicrobial Therapy to Prevent Surgical Site Infections
- NCT06533111 · 4,500 participants · NA
Improving Surgical Patient Outcomes Through Implementation of a SemiStructured Intraoperative Anesthesia Handoff Tool
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia