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Comparison · NCT00462306-41296a66

Pregnant Women vs Non-Pregnant Women: Positive Berlin Questionnaire Indicative of Sleep Disordered Breathing

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Pregnant Women vs Non-Pregnant Women: Positive Berlin Questionnaire Indicative of Sleep Disordered Breathing. Trial comparisons, record NCT00462306-41296a66. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00462306-41296a66

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.330.3150.344wilson
Risk in group 20.1910.1590.227wilson
Risk difference, group 1 minus group 20.1390.09950.174newcombe hybrid score
Risk ratio, group 1 over group 21.731.442.08log
Odds ratio, group 1 over group 22.081.652.63log
Number needed to treat, for one more participant with the outcome on Pregnant Women than on Non-Pregnant Women7.25.7510.1from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Pregnant Women1,3434,074OG000
Group 2Non-Pregnant WomenNon-pregnant women undergoing a surgical procedure96503OG001

Outcome

Type
PRIMARY
Title
Positive Berlin Questionnaire Indicative of Sleep Disordered Breathing
Description
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 if 2 or more categories are positive.
Time frame
1-2 minutes
Population
Pregnant Women presenting to Prentice Women's Hospital or non-pregnant women or childbearing age presenting for ambulatory surgery from 10/2005 to 9/2007 were selected randomly and asked to complete the survey.

Source ClinicalTrials.gov

Trial

Title
Incidence of Obstructive Sleep Apnea in Pregnancy
NCT number
NCT00462306
Phases
Conditions
Obstructive Sleep Apnea, Pregnancy
Interventions
Survey: Berlin questionnaire
Lead sponsor
Northwestern University
Results first posted
2011-05-25

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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