Skip to content

Comparative study of the accuracy of the portable GOSPT2000 lung function instrument

Variation of central- and peripheral-airway function variables in healthy subjects: data from 7-day diurnal and nocturnal home monitoring with electronic portable spirometer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100050355
Enrollment
Unknown
Registered
2021-08-26
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

chronic airway disease

Interventions

Gold Standard:Results of a major pulmonary function test performed in the hospital
lung&#32
meter(GOSPT2000)test&#32

Sponsors

Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years; 2. No clinical symptoms within 8 weeks; 3. The physical examination report within 1 month is normal (including routine laboratory tests such as blood routine, blood biochemical tests, tumor markers such as CEA, AFP, etc.), B-ultrasound, electrocardiogram, chest high-resolution CT are all normal; 4. No smoking history in their lifetimes, no allergic medical history such as allergic rhinitis or allergic dermatitis; 5. No chronic respiratory disease; 6. No previous pulmonary function test experience; 7. No medical background.

Exclusion criteria

Exclusion criteria: 1. Subjects were excluded if they had systemic diseases, including presence of unstable cardiovascular status, diabetes, gastroesophageal reflux, nausea, vomiting, abdominal pain and stress urinary incontinence; 2. Surgery of the chest, abdomen, or eye within the past 2 weeks; 3. History of syncope associated with forced exhalation, and unsuitable for lung function examination; oral or facial pain aggravation when chewing; 4. Subjects who had mental disease and cognitive disorders were also excluded.

Design outcomes

Primary

MeasureTime frame
Sensitivity (SEN);Specificity (SPE);Accuracy (ACC);Area under the curve (AUC) of Receiver operating characteristic curve (ROC);

Countries

China

Contacts

Public ContactZhang Min

Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

maggie_zhangmin@163.com+86 13482345145

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026