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Correlation Between Patient and Family Completed Epworth Sleepiness Scale Scores with Obstructive Sleep Apnea Severity Based on Polysomnography

Correlation Between Patient and Family Completed Epworth Sleepiness Scale Scores with Obstructive Sleep Apnea Severity Based on Polysomnography - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/10/096739
Enrollment
80
Registered
2025-10-31
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J989- Respiratory disorder, unspecified

Interventions

Intervention1: Nil: Nil

Sponsors

Fortis Hospitals Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients reporting symptoms suggestive of OSA, including but not limited to: Loud snoring, witnessed apnoeas (breathing pauses during sleep), gasping or choking during sleep, excessive daytime sleepiness, morning headaches, unrefreshing sleep, fatigue, difficulty concentrating, irritability PSG: Patients subjected to overnight diagnostic polysomnography (PSG) (home study or hospital-based study) within 4 weeks of being evaluated for inclusion in the study. Family Member Availability: Patients who have a family member willing to participate in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Family Reported ESS Correlating better with the OSA Severity (AHI) than patient reported ESSTimepoint: 7 Days—

Secondary

MeasureTime frame
Family Reported ESS Correlating better with PSG Parameters (ODI and Arousal Index) than Patient reported ESSTimepoint: 7 Days—

Countries

India

Contacts

Public ContactDr Ayushi Sinha

Fortis Hospitals Limited

mrinal.sircar@fortishealthcare.com9871292226

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026