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The Fever Clinic Acute Respiratory Cohort (FACTS): A Prospective Real-World Cohort Study of Patients Presenting to Fever Clinics: Clinical Features, Laboratory and Radiographic Findings, and Long-Term Outcomes of Acute Respiratory Infections

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

This prospective cohort study aims to characterize the natural progression and outcomes of acute respiratory infections among patients presenting to fever clinics. At enrollment, patients' clinical symptoms, laboratory findings, and chest imaging data will be collected. Longitudinal follow-up will be conducted to evaluate disease progression, complications, and long-term outcomes. As an observational study, no interventions are involved; all patients receive routine clinical management as directed by their attending physicians. This real-world study design enables the assessment of the natural course of acute respiratory infections and the identification of factors associated with clinical outcomes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years (based on official identification document).

• Presence of fever at the time of visit or within 24 hours prior to the visit, defined as a documented temperature of ≥37.3°C axillary/tympanic, ≥37.8°C orally, or ≥38.0°C rectally.

• The primary cause of fever, as determined by the attending physician, is a respiratory tract infection.

• Blood draw is required as part of standard clinical care.

• Ability to comprehend the study's purpose, procedures, and potential risks, and willingness to provide written informed consent.

Locations
Other Locations
China
Huadong hospital
RECRUITING
Shanghai
Contact Information
Primary
YingGang Zhu, Doctor
robinzyg@gmail.com
+8618001637153
Time Frame
Start Date: 2025-10-10
Estimated Completion Date: 2028-10
Participants
Target number of participants: 1000
Treatments
Pneumonia Cohort
Non-Pneumonia Cohort
Related Therapeutic Areas
Sponsors
Collaborators: Huadong Hospital
Leads: Fudan University

This content was sourced from clinicaltrials.gov