About this trial

The objective of this study is to compare the effectiveness of batten grafts plus septoplasty and turbinate reduction (intervention arm) compared to septoplasty and turbinate reduction alone (control arm), both in terms of subjective and objective assessments.

Eligibility criteria

Qualifiers

Be age 18 or above

Able to provide written informed consent

Have an indication for batten graft, septoplasty and turbinate reduction according to prevailing surgical practices.

Septal deviation must be present on direct or endoscopic examination

Disqualifiers

Septal perforation

History of previous functional rhinoplasty or sinus or septal surgery

Patients who are selected for concurrent aesthetic/cosmetic rhinoplasty

Untreated allergic rhinitis or allergic rhinitis unresponsive to medical management

Trial design

Treatments tested in this trial

  • Batten batten graft
  • Septoplasty
  • Inferior Turbinate Reduction

Treatment groups

96 Participants
are divided into 2 treatment groups

Locations

3
Poplar Bluff Regional Medical Center63901, Poplar BluffMissouri, United States
Lenox Hill Hospital/Staten Island University Hospital10075, New YorkNew York, United States
Staten Island University Hospital10305, Staten IslandNew York, United States

Sponsors and collaborators

Northwell Health

Lead sponsor