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Not yet recruitingNCT07015255Updated Jun 19, 2025

Assessing the Burden of Respiratory Syncytial Virus (RSV)

An observational study in Respiratory Syncytial Virus (RSV) Infection, Acute Lower Respiratory Tract Infections and Bronchiolitis, sponsored by Abu Dhabi Health Services Company. Not yet recruiting at 1 site in United Arab Emirates. Per ClinicalTrials.gov, last updated 2025-06-19.

Sponsored by Abu Dhabi Health Services Company · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2026, 5 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
1,500
Sex
All
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Study summary

This study examines the impact of Respiratory Syncytial Virus (RSV) on people of all ages, from infants to the elderly. It uses hospital records collected between January 2018 and December 2024 to understand:

  • How often does RSV occur
  • Who is most at risk
  • The long-term and financial effects of RSV
Read the detailed description

This study is designed to analyze the impact of Respiratory Syncytial Virus (RSV) across different age groups. It focuses on how often RSV occurs, who is most at risk, and its long-term and financial effects. The study uses existing hospital records from SEHA facilities between January 2018 and December 2024. This is a retrospective observational study, meaning no new tests or treatments are given. Researchers look at medical records from past patients who were diagnosed with RSV. Anonymized data is collected from SEHA's Electronic Medical Records (EMR) and laboratory systems. Only patients with confirmed RSV infections are included.

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Conditions studied

  • Respiratory Syncytial Virus (RSV) Infection
  • Acute Lower Respiratory Tract Infections
  • Bronchiolitis
  • Pneumonia
  • Chronic Respiratory Conditions

Keywords

  • Respiratory Syncytial Virus
  • RSV
  • RSV Infection
  • RSV in Infants
  • RSV in Adults
  • RSV Hospitalization
  • RSV Epidemiology
  • RSV Burden
  • RSV Risk Factors
  • Retrospective Study
  • Observational Study
  • ICU Admissions
  • RSV Mortality
  • RSV Cost Analysis
  • RSV Complications
  • Asthma and RSV
  • Bronchiolitis
  • Pneumonia
  • Recurrent Wheezing
  • RSV Surveillance
  • RSV-Related Comorbidities
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In context

Infections

2,093 studies on the registry are indexed under Infections; 364 are open to participants now.

This study's planned enrollment of 1,500 is above the median of 300 across 685 observational studies indexed under Infections.

Browse Infections studies →

Lead sponsor

Abu Dhabi Health Services Company is the lead sponsor of 9 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

This study includes all patients of any age who have a laboratory-confirmed diagnosis of Respiratory Syncytial Virus (RSV) infection recorded in the SEHA electronic medical records between January 2018 and December 2024. The population spans from newborn infants to elderly adults, including those with underlying medical conditions such as chronic lung disease, heart disease, immunosuppression, and other comorbidities that may influence RSV severity. Both hospitalized patients and those diagnosed in outpatient settings within SEHA healthcare facilities are included. The study aims to represent the full spectrum of RSV disease burden, clinical outcomes, risk factors, long-term health impacts, and healthcare costs across diverse demographic groups in the UAE.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients of all ages with a confirmed diagnosis of RSV infection
  • Patients admitted to a SEHA hospital or healthcare facility between January 2018 and December 2024
  • Patients with documented data in the SEHA electronic medical record (EMR) system

Exclusion criteria

Exclusion Criteria:

  • Patients with suspected RSV infection that is not laboratory-confirmed
  • Patients without sufficient data in the SEHA EMR system
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
1,500 participants (estimated)
Patient registry
No

Groups and cohorts

  • Infants, adults, elderly, and high-risk patients with confirmed RSV infection (2018-2024).

    This retrospective study includes patients of all ages with confirmed Respiratory Syncytial Virus (RSV) infection from January 2018 to December 2024, categorized into four cohorts: (1) Infants and young children, including those with risk factors such as prematurity, low birth weight, and chronic lung or heart disease; (2) Adults aged 18-64 years with or without comorbidities; (3) Elderly adults aged 65 and older, with focus on severe outcomes and mortality; and (4) High-risk individuals across all age groups with underlying conditions such as asthma, COPD, diabetes, immunosuppression, Down syndrome, or cystic fibrosis. No interventions are administered; the study analyzes existing data to assess RSV burden, ICU admissions, long-term health impacts, and associated healthcare costs.

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What researchers measure

Primary outcomes

  1. Burden of RSV Infection Across All Age Groups

    Measurement of the incidence of confirmed RSV infections in patients of all ages using SEHA hospital data from January 2018 to December 2024.

    Time frame: January 2018 - December 2024

  2. Burden of RSV Infection Across All Age Groups

    Measurement of the prevalence of confirmed RSV infections in patients of all ages using SEHA hospital data from January 2018 to December 2024.

    Time frame: January 2018 - December 2024

Secondary outcomes

  1. Identification of Risk Factors for Severe RSV Infection

    Analysis of clinical, demographic, and comorbidity data to identify key risk factors associated with severe RSV infection outcomes.

    Time frame: January 2018 - December 2024

  2. Proportion of Hospital Admissions Due to RSV

    Evaluation of the percentage of total hospital admissions attributed to RSV infections.

    Time frame: January 2018 - December 2024

  3. ICU Admission Rates for RSV-Infected Patients

    Measurement of the proportion of RSV patients requiring ICU care.

    Time frame: January 2018 - December 2024

  4. Financial Burden of RSV Infection

    Assessment of direct medical costs associated with RSV hospitalization and ICU care.

    Time frame: January 2018 - December 2024

  5. Incidence of Recurrent Wheezing and Asthma Diagnosis Following RSV Infection

    Evaluation of long-term respiratory complications, specifically: 1. Clinically diagnosed asthma using standardized clinical criteria (e.g., based on ICD-10 codes or physician diagnosis recorded in medical records) 2. Recurrent wheezing episodes, defined as ≥3 wheezing episodes confirmed by clinical examination or parent report within 12 months post-infection, assessed via structured caregiver questionnaires and medical record review.

    Time frame: Up to 12 months post-infection

  6. RSV-Associated Mortality Rates

    Analysis of death rates among RSV-positive patients, including 30-day mortality post-admission.

    Time frame: January 2018 - December 2024

  7. Long-Term Respiratory Outcomes Following RSV Infection

    Evaluation of post-RSV respiratory complications such as asthma and recurrent wheezing.

    Time frame: Up to 12 months post-infection

07

Study locations

1 site
08

References and documents

Publications

  • Felton DA. A time of 'firsts'. J Prosthodont. 2004 Mar;13(1):1-2. doi: 10.1111/j.1532-849X.2004.04011.x. No abstract available. PubMed 15032890 ↗
  • Zhou H, Thompson WW, Viboud CG, Ringholz CM, Cheng PY, Steiner C, Abedi GR, Anderson LJ, Brammer L, Shay DK. Hospitalizations associated with influenza and respiratory syncytial virus in the United States, 1993-2008. Clin Infect Dis. 2012 May;54(10):1427-36. doi: 10.1093/cid/cis211. Epub 2012 Apr 10. PubMed 22495079 ↗
  • Hall CB, Weinberg GA, Iwane MK, Blumkin AK, Edwards KM, Staat MA, Auinger P, Griffin MR, Poehling KA, Erdman D, Grijalva CG, Zhu Y, Szilagyi P. The burden of respiratory syncytial virus infection in young children. N Engl J Med. 2009 Feb 5;360(6):588-98. doi: 10.1056/NEJMoa0804877. PubMed 19196675 ↗
  • Wassmer SC, Lepolard C, Traore B, Pouvelle B, Gysin J, Grau GE. Platelets reorient Plasmodium falciparum-infected erythrocyte cytoadhesion to activated endothelial cells. J Infect Dis. 2004 Jan 15;189(2):180-9. doi: 10.1086/380761. Epub 2004 Jan 9. PubMed 14722881 ↗
  • Callen A, Diener-West M, Zeitlin PL, Rubenstein RC. A simplified cyclic adenosine monophosphate-mediated sweat rate test for quantitative measure of cystic fibrosis transmembrane regulator (CFTR) function. J Pediatr. 2000 Dec;137(6):849-55. doi: 10.1067/mpd.2000.109198. PubMed 11113843 ↗
  • Falsey AR, Hennessey PA, Formica MA, Cox C, Walsh EE. Respiratory syncytial virus infection in elderly and high-risk adults. N Engl J Med. 2005 Apr 28;352(17):1749-59. doi: 10.1056/NEJMoa043951. PubMed 15858184 ↗
  • Joury J, Al Kaabi N, Al Dallal S, Mahboub B, Zayed M, Abdelaziz M, Onwumeh-Okwundu J, Fletcher MA, Kumaresan S, Ramachandrachar BC, Farghaly M. Retrospective Analysis of RSV Infection in Pediatric Patients: Epidemiology, Comorbidities, Treatment, and Costs in Dubai (2014-2023). J Health Econ Outcomes Res. 2024 Nov 5;11(2):133-144. doi: 10.36469/001c.123889. eCollection 2024. PubMed 39575134 ↗
  • Nair H, Nokes DJ, Gessner BD, Dherani M, Madhi SA, Singleton RJ, O'Brien KL, Roca A, Wright PF, Bruce N, Chandran A, Theodoratou E, Sutanto A, Sedyaningsih ER, Ngama M, Munywoki PK, Kartasasmita C, Simoes EA, Rudan I, Weber MW, Campbell H. Global burden of acute lower respiratory infections due to respiratory syncytial virus in young children: a systematic review and meta-analysis. Lancet. 2010 May 1;375(9725):1545-55. doi: 10.1016/S0140-6736(10)60206-1. PubMed 20399493 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 19, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07015255
Lead sponsor
Abu Dhabi Health Services Company
Responsible party
Sponsor
First posted
Jun 11, 2025
Start date
Jun 2025 (estimated)
Primary completion
Jun 2026 (estimated)
Completion
Jun 2026 (estimated)
Last update
Jun 19, 2025

Study contacts

Lina Khairy, MD
Contact
o-lkhayri@seha.ae
+971589111897
Alina Naeem, MBBS, MS
Contact
alina.naeem@purehealth.ae
+971566089799
Salah Eldin Hussein, MD
study director · Abu Dhabi Health Services Company-SEHA
Nawal Alkaabi, MD
principal investigator · Abu Dhabi Health Services Company-SEHA

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

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