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A prospective study of the effect of functional endoscopic sinus surgery (FESS) on the recovery of olfactory function in patients with chronic sinusitis

A prospective study of the effect of functional endoscopic sinus surgery (FESS) on the recovery of olfactory function in patients with chronic sinusitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100047644
Enrollment
Unknown
Registered
2021-06-21
Start date
2021-06-21
Completion date
Unknown
Last updated
2022-02-28

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

Conditions

Olfaction dysfunction

Interventions

Case group:Nil

Sponsors

The First Affiliated Hospital of Air Force Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects must voluntarily sign an informed consent form; 2. Age >= 18 years old and <= 65 years old; 3. The diagnosis of the subject meets the diagnostic criteria of chronic sinusitis with or without nasal polyps in the ''Chinese Guidelines for the Diagnosis and Treatment of Chronic Sinusitis (2018)''; 4. The subject meets the surgical indications of the "Chinese Guidelines for the Diagnosis and Treatment of Chronic Sinusitis (2018)"; 5. No previous history of nose surgery.

Exclusion criteria

Exclusion criteria: 1. Those who voluntarily ask to withdraw, have poor compliance and cannot cooperate with regular follow-up and treatment observers; 2. Subjects have the following diseases: cystic fibrosis, congenital ciliary dyskinesia, nasal tumors, nasal and facial deformities, history of nasal and facial trauma causing nasal cavity obstruction, invasive or non-invasive fungal sinusitis, sinus anatomy abnormal patients; 3. Accompanied by severe metabolic, cardiovascular, immune, neurological, blood, digestive, cerebrovascular or respiratory diseases, or diseases that may affect the results of the research or affect the safety of the subjects evaluated by the researcher; 4. Severe systemic complications, orbital and intracranial complications occurred during and after the operation; 5. Those who are currently participating in other clinical research or have participated in other clinical research within 30 days, or directly participating in this research; 6. Those who have a history of mental illness, confrontational personality, bad motivation, suspiciousness, or other emotional or intellectual problems that may affect the informed effectiveness of participating in the research.

Design outcomes

Primary

MeasureTime frame
Quality of life level of chronic sinusitis;Pain;Olfactory recovery level;

Countries

China

Contacts

Public ContactChen Fuquan

The First Affiliated Hospital of the Air Force Medical University

chenfq@fmmu.edu.cn+86 13772079206

Outcome results

None listed

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