Suture-based, Minimally Invasive Technique Used to Correct NSD

Sponsor
Stanford University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04891263
Collaborator
(none)
10
2
1
18
5
0.3

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Suture-Septoplasty
  • Device: Surgical suture
N/A

Detailed 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.

We 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Safety and Efficacy of Suture-Septoplasty for Chronic, Durable Correction of Nasal Septal Deviation Causing Nasal Obstruction Symptoms
Anticipated Study Start Date :
Jun 1, 2021
Anticipated Primary Completion Date :
Jun 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Suture-Septoplasty

Participants will receive suture-septoplasty technique, and will be followed for three months postoperatively.

Procedure: Suture-Septoplasty
Patients receive suture-septoplasty for repair of nasal septal deviation.

Device: Surgical suture
Suture used for closure during septoplasty surgery.
Other Names:
  • PDS suture
  • Outcome Measures

    Primary Outcome Measures

    1. Nasal Obstruction Symptom Evaluation (NOSE) score [baseline, month 3]

      Mean change from baseline

    Secondary Outcome Measures

    1. Sino-Nasal Outcome Test (SNOT)-22 score [baseline, month 3]

      Mean change from baseline

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Stanford Ambulatory Surgery Center, Stanford Hospital Palo Alto California United States 94304
    2 Stanford Sinus Center/ Adult Comprehensive ENT Clinic Stanford California United States 94305

    Sponsors and Collaborators

    • Stanford University

    Investigators

    • Principal Investigator: Jayakar V Nayak, M.D., Ph.D., Associate Professor of Otolaryngology - Head & Neck Surgery, Stanford University Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Jayakar Nayak, Associate Professor of Otolaryngology - Head & Neck Surgery (OHNS) and, by courtesy, of Neurosurgery at the Stanford University Medical Center, Stanford University
    ClinicalTrials.gov Identifier:
    NCT04891263
    Other Study ID Numbers:
    • 57545
    First Posted:
    May 18, 2021
    Last Update Posted:
    May 18, 2021
    Last Verified:
    May 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Keywords provided by Jayakar Nayak, Associate Professor of Otolaryngology - Head & Neck Surgery (OHNS) and, by courtesy, of Neurosurgery at the Stanford University Medical Center, Stanford University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 18, 2021