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Septorhinoplasty With and Without Nasal Packing

Comparative Study Septorhinoplasty With and Without Nasal Packing in Operated patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201507051138N21
Enrollment
70
Registered
2015-08-21
Start date
2015-07-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Septorhinoplasty. -

Interventions

Intervention 1: 35 patients underwent septorhinoplasty with packing in Time Period 1, septum will be sewn with yarn 3 0 vicryl. Suture running will be performed by the surgeon.Mesh treated with tetrac
Treatment - Surgery
Treatment - Drugs
35 patients underwent septorhinoplasty with packing in Time Period 1, septum will be sewn with yarn 3 0 vicryl. Suture running will be performed by the surgeon.Mesh treated with tetracycline will be a
35 patients underwent septorhinoplasty without packing in Time Period 2, Each Time Period is one Month. During septum surgery, septum will be sewn with yarn 3 0 vicryl. Suture running will be perform

Sponsors

Guilan University of Medical Science, Vice Chancellor for Resarch
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:18-50 years; exclusion criteria: patients with underlying disease (such as diabetes, heart problems, high blood pressure, and blood dyscrasia); a history of nasal polyps; drug abuse; nasal allergy; blood-thinning drugs such as aspirin; Patients with a history of nasal septum and turbinate surgery; nasal deformity curved; perforated septum; saddle-shaped deformity;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Ecchymosis. Timepoint: Two days after surgery. Method of measurement: Based on clinical examination.;Bleeding. Timepoint: Two days after surgery,One week after surgery,One Month after surgery. Method of measurement: Based on clinical examination.;Patient satisfaction. Timepoint: Two days after surgery,One week after surgery,One Month after surgery. Method of measurement: Based on clinical examination.;Edema. Timepoint: Two days after surgery. Method of measurement: Based on clinical examination.;Hematoma. Timepoint: Two days after surgery. Method of measurement: Based on clinical examination.;Mucosal lesions. Timepoint: One week after surgery. Method of measurement: Based on clinical examination.;Difficulty breathing. Timepoint: One week after surgery. Method of measurement: Based on clinical examination.;Pain. Timepoint: , One week after surgery. Method of measurement: Based on clinical examination.;Secondary infection. Timepoint: One week after surgery,One Month after surgery. Method of measurement: Based on clinical examination.;Granuloma. Timepoint: One week after surgery. Method of measurement: Based on clinical examination.;Mucosal Adhesion in Nasal Airway. Timepoint: One Month after surgery. Method of measurement: Based on clinical examination.;Nasal valve stenosis. Timepoint: One week after surgery. Method of measurement: Based on clinical examination.;Marginal incision site. Timepoint: One Month after surgery. Method of measurement: Based on clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Ali Faghih habibi

Guilan University of Medical Science

Dr.faghih.habibi@gmail.com+98 13 3322 5242

Outcome results

None listed

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