Skip to content

Efficacy of Oil-Coated Nasal Stents Versus Bare Metal Stents for Nasal Packing After Septoplasty: A Multicenter, Double-Blind, Randomized Controlled Trial

Efficacy of Oil-Coated Nasal Stents Versus Bare Metal Stents for Nasal Packing After Septoplasty: A Multicenter, Double-Blind, Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122624
Enrollment
Unknown
Registered
2026-04-15
Start date
2026-04-22
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

nasal septum

Interventions

Experimental group:Oiled coating stent
Control group:Bare metal stent

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 to 65 years old; 2. The chief complaint is nasal congestion, and the sinus CT shows a deviated nasal septum. There are indications for surgery to correct the deviated nasal septum 3. No other treatment methods were employed;

Exclusion criteria

Exclusion criteria: 1. Patients who have previously undergone nasal surgery and those who are scheduled to undergo sinus surgery; 2. Women who are already pregnant, or are preparing to become pregnant or are in the lactation period; 3. Patients with severe systemic diseases or chronic conditions, such as coagulation disorders, immune dysfunction, tumors, chronic heart failure, severe depression or other mental disorders, should be combined. 4. Relatives of researchers or managers; 5. Some members of the family have already participated in this study; 6. In the past two weeks, had acute diseases such as upper respiratory tract infection or fever; 7. Those who are unable or unwilling to cooperate with the treatment plan and the nasal examination for any reason.

Design outcomes

Primary

MeasureTime frame
Efficiency of removal after filling is completed;

Secondary

MeasureTime frame
Quality of life score during the filling period (SNOT-22 nasal symptom scale);NOSE Nasal Obstruction Symptom Scale;Comfort assessment;

Countries

China

Contacts

Public ContactLiu Junxiu

Peking University First Hospital

liujunxiusanyuan@sina.com+86 13439607635

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026