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Clinical Trials/NCT01322945
NCT01322945
Completed
Not Applicable

Observational Study of Nasal Outcomes Following Endonasal Surgery for Anterior Skull Base Lesions

St. Joseph's Hospital and Medical Center, Phoenix1 site in 1 country94 target enrollmentOctober 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pituitary Tumors
Sponsor
St. Joseph's Hospital and Medical Center, Phoenix
Enrollment
94
Locations
1
Primary Endpoint
Change in Mean Survey Response From Baseline to 90 Days Post Surgery
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this study is to evaluate patient nasal outcome following endo-nasal surgery. This type of surgery is conducted for pituitary and skull base tumors. There is no published data on trauma to the nose during surgery and how it impacts nasal functioning. The investigators propose to develop a survey and administer it to patients before and after surgery to learn about their perception of nasal functioning.

Detailed Description

A 9-item patient survey (the ASK Nasal Inventory) focusing on the most common postoperative complaints, such as crusting, sinusitis, pain, and ease of breathing, was developed by the anterior skull base team at the Barrow Neurological Institute. Content was validated in structured patient interviews by four subject-matter experts with both endonasal and control groups. Eligible patients for the control group included patients undergoing any neurosurgical procedure requiring anesthesia that did not involve the endonasal corridor, such as spinal decompression procedures, craniotomies for trigeminal neuralgia, and shunting procedures. This survey was self-administered pre- and 3 months post-surgery.

Registry
clinicaltrials.gov
Start Date
October 2010
End Date
June 2011
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
St. Joseph's Hospital and Medical Center, Phoenix
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adults with planned endonasal surgery for pituitary tumor or skull base lesion

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in Mean Survey Response From Baseline to 90 Days Post Surgery

Time Frame: Baseline, 90 days post surgery

Mean survey response at 90 days post surgery between the control patients and the endonasal surgery patients using the Anterior skull base nasal inventory (ASK Nasal Inventory. A 5-point Likert scale for each question on the ASK Nasal inventory measures frequency of nasal symptoms where 1=never, 2= a little of the time, 3=some of the time, 4=most of the time, 5= all of the time. Total mean Likert scores were compared in the endonasal group to the control group after surgery. Scores range from minimum of 9 to maximum of 45. The lower the score the fewer the nasal complaints.

Secondary Outcomes

  • Test-retest Reliability of the ASK Nasal Inventory(90 days and 120 days post surgery)

Study Sites (1)

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