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Treatment of deviation of nasal septum with transfixion suture of nasal septum and nasal packing: a prospective randomized controlled trial

Treatment of deviation of nasal septum with transfixion suture of nasal septum and nasal packing: a prospective randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030873
Enrollment
Unknown
Registered
2020-03-16
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-03-30

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

Conditions

nasal septum deviation

Interventions

experimental group:continuous transfixion suture

Sponsors

Ophthalmotolaryngology Hospital Affiliated of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients with septal deviation 1. Get patients informed consent befoe clinical research; 2. Men and women with aged 18-50 years and clinically evident of nasal septum deviation; 3. Patients with at least one year's history of deviation of nasal septum with or without hypertrophy of bilateral inferior turbinate; 4. With nasal septum deviation confirmed by CT; 5. Patients willing and able to follow the trial protocol.

Exclusion criteria

Exclusion criteria: 1. With risk factor for postoperative hemorrhage including high blood pressure, diabetes, blood disease; 2. Patients receive other nose surgery at the same time; 3. Pregnant or breast-feeding during the trial period; 4. Patients with allergic rhinitis; 5. Patient have previous nose surgery; 6. Patients with depression and other mental health conditions; 7. With depression and other mental health conditions; 8. Any clinically relevant condition that the investigator believes will interfere with the evaluation of the trial or the safety of the subject; 9. Have business or personal relationship with test personnel or sponsor directly involved in test implementation.

Design outcomes

Primary

MeasureTime frame
Vas scale;

Countries

China

Contacts

Public ContactJuan Liu

Ophthalmotolaryngology Hospital Affiliated to Fudan University

juanzi861018@126.com+86 18917786191

Outcome results

None listed

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