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Endoscopic Sinus Surgery (ESS) Combined with Posterior Nasal Neurectomy and ESS alone in the Treatment of Eosinophilic Chronic Rhinosinusitis with Nasal Polyps: A Randomized Controlled Study

Endoscopic Sinus Surgery (ESS) Combined with Posterior Nasal Neurectomy and ESS alone in the Treatment of Eosinophilic Chronic Rhinosinusitis with Nasal Polyps: A Randomized Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099317
Enrollment
Unknown
Registered
2025-03-21
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Eosinophilic Chronic Rhinosinusitis with Nasal Polyps

Interventions

Control group:ESS
Experimental group:ESS with posterior nasal neurectomy (PNN)

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Age 18–60 years, both sexes. 2.Meet the EPOS2020 diagnostic criteria for chronic rhinosinusitis with nasal polyps (CRSwNP). 3.Refer to JESREC diagnostic criteria: >=11 points indicate eosinophilic (EOS) infiltration type CRSwNP. 4.Peripheral blood total IgE >=100 U/mL. 5.Pathological tissue EOS >10/high-power field (HPF).

Exclusion criteria

Exclusion criteria: 1.Patients who have used any form of oral hormones, antibiotics, or antihistamines within 4 weeks before enrollment. 2.Patients who have a history of upper respiratory tract infection or asthma attack within 2 weeks before enrollment. 3.Pregnant or lactating patients. 4.Patients with severe underlying diseases (poorly controlled diabetes, hypertension, rheumatic immune system diseases requiring long - term use of hormones, etc.), or those with other tumors or systemic diseases. 5.Patients who are currently participating in clinical trials, or have participated in other clinical trials within the past 30 days, or are personnel involved in this study. 6.People with a history of mental illness, or other emotional or intellectual problems, or those who cannot understand the informed consent or subjective assessment forms due to language problems.

Design outcomes

Primary

MeasureTime frame
Lund-Kennedy score;

Secondary

MeasureTime frame
VAS score;SNOT-22 score;Time Cost;Economic Cost;Adverse reaction;

Countries

China

Contacts

Public ContactXifu Wu

The Third Affiliated Hospital of Sun Yat-sen University

wuxif@mail.sysu.edu.cn+86 20 8525 2239

Outcome results

None listed

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