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Suture-based, Minimally Invasive Technique Used to Correct NSD

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Stanford University

Status

Terminated

Conditions

Nasal Obstruction
Nasal Septum; Deviation, Congenital

Treatments

Procedure: Suture-Septoplasty
Device: Surgical suture

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Nasal Septal Deviation (NSD) is one of the most common indications for surgery seen by ENT physicians, however, correction requires open surgery which is associated with several weeks of recovery. The purpose of this study is to elucidate whether a suture-based, minimally invasive technique can be used to safely and effectively address NSD.

Full description

Nasal obstruction due to structural issues such as nasal septal deviation (NSD) is remarkably common. NSD is caused by warping of the midline cartilage and bone of the septum, which starts between the 2 nostrils, and extends 7 cm posteriorly to the nasopharynx. This crooked or deviated conformation in the nasal septum cartilage and/or bone leads to physical blockade of normal airflow through the nose, often leading to complaints of nasal congestion, sleep disturbance, exercise limitations, and even poor compliance with CPAP mask use for treatment of obstructive sleep apnea (OSA). To correct this structural issue in symptomatic patients, septoplasty surgery under general anesthesia is typically advocated.

As an alternative to standard septoplasty, there are rare reports of simplified suture techniques that may be used to straighten the nasal septal cartilage. However, virtually all published studies to our knowledge have still required 1) some degree of cartilage/bone excision, which can destabilize the nasal support framework, and 2) use of non-locking sutures which can break, provide insufficient support, and be technically challenging given that it requires knot tying within the narrow nasal cavity corridors.

The investigators have demonstrated in benchtop models that similar results to standard septoplasty techniques can may be achieved with the use of a non-retractable suture without the need for cartilage excision. This technique, therefore, could allow for a simple, and knotless, minimally invasive way to improve and/or correct symptomatic NSD.

Enrollment

4 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age ≥ 18
  • Patients from all ethnic and geographic backgrounds within the Stanford Sinus Center with symptomatic NSD
  • Primary patients with NSD without past septum surgery
  • Patients who have failed maximum medical therapy
  • Patients whose symptoms, examination and/or imaging findings are sufficiently severe as to warrant septoplasty as determined by the treating surgeon

Exclusion criteria

  • Age < 18
  • Recent surgery of any kind (<1 month)
  • Inpatients
  • Previous nasal septum surgery

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

4 participants in 1 patient group

Suture-Septoplasty
Experimental group
Description:
Participants will receive suture-septoplasty technique, and will be followed for three months postoperatively.
Treatment:
Device: Surgical suture
Procedure: Suture-Septoplasty

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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