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Inferior Turbinate Surgery in Rhinoseptoplasty: a Randomized Clinical Trial With Quality of Life Outcomes

Inferior Turbinate Surgery in Rhinoseptoplasty: a Randomized Clinical Trial With Quality of Life and Acoustic Rhinometry Outcomes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01457638
Enrollment
50
Registered
2011-10-24
Start date
2010-12-31
Completion date
2011-10-31
Last updated
2019-01-17

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

Conditions

Nasal Obstruction, Rhinoplasty, Rhinoseptoplasty, Turbinate Surgery, Quality of Life

Keywords

nasal obstruction, rhinoplasty, turbinate surgery, quality of life, acoustic rhinometry

Brief summary

The purpose of this study is to determine whether inferior turbinate surgery during rhinoseptoplasty is effective in improving quality of life and acoustic rhinometry outcomes.

Interventions

During rhinoseptoplasty inferior turbinate submucosal cauterization is performed.

PROCEDURENo iInferior turbinate surgery

During rhinoseptoplasty no intervention is done in inferior turbinates

Sponsors

Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Older than 15 years old; * Nasal obstruction and nasal aesthetics complaints;

Exclusion criteria

* Previous septoplasty, turbinates intervention and/or rhinoplasty; * Association of other surgical procedures in the same surgical time, as functional endoscopic sinus surgery, blepharoplasty, mentoplasty or otoplasty; * Inferior turbinate hypertrophy as the isolated cause of nasal obstruction (no septum deviation or internal valve collapse)

Design outcomes

Primary

MeasureTime frameDescription
Nasal Obstructive Symptoms Evaluation Scale3 months postopSpecif instrument for evaluation of quality of life related to nasal obstruction

Secondary

MeasureTime frameDescription
World Health Organization Quality of Life (WHOQOL)3 months postopquality of life instrument
Rhinoplasty Outcomes Evaluation3 months postopquality of life for rhinoplasty patients
Allergic Conjunctivitis3 months postopAt 90 posoperative day patients were asked if they had allergic conjunctivitis for more than one hour a day on most days, or not.
Nasal Rhinorrea3 months postopAt 90 posoperative day patients were asked if they had nasal rhinorrea for more than one hour a day on most days, or not.
Acoustic Rhinometry3 months post-op
Nasal Sneeze3 months postopAt 90 posoperative day patients were asked if they had nasal sneeze for more than one hour a day on most days, or not.
Topic nasal corticosteroid3 monthsAt 90 posoperative day patients were asked if they were using topic nasal corticosteroid or not.
Oral antihistamine3 monthsAt 90 posoperative day patients were asked if they had used oral antihistamine in the past 30 days or not
Nasal pruritis3 months posoptAt 90 posoperative day patients were asked if they had nasal pruritis for more than one hour a day on most days, or not.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026