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Clinical Trials/NCT04087902
NCT04087902
Recruiting
Not Applicable

A Prospective Longitudinal Quality of Life Study in Patients Undergoing Endoscopic Endonasal Skull Base Surgery

Ohio State University1 site in 1 country400 target enrollmentJuly 16, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pituitary Tumor
Sponsor
Ohio State University
Enrollment
400
Locations
1
Primary Endpoint
PROMIS-29 quality of life outcome measures for patients undergoing endoscopic endonasal surgeries.
Status
Recruiting
Last Updated
10 months ago

Overview

Brief Summary

This is a prospective longitudinal study to access postoperative 2-year quality of life in patients who undergo endonasal endoscopic approach surgeries of the skull base.

Detailed Description

This is a prospective single-institution longitudinal study to access quality of life in patients who undergo endonasal endoscopic approach surgeries of the skull base. Patients will be followed before surgery and up to twenty-four months post-surgery. The primary goal of the study is to assess the alterations to patient quality of life following endoscopic endonasal surgery using modern sinonasal reconstruction techniques. Secondary goals are to better understand the time course of normal healing and patient/procedural risk factors associated with poorer quality of life outcomes.

Registry
clinicaltrials.gov
Start Date
July 16, 2019
End Date
December 31, 2025
Last Updated
10 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kyle Wu

Assistant Professor, Neurological Surgery

Ohio State University

Eligibility Criteria

Inclusion Criteria

  • Patient is scheduled to undergo endoscopic endonasal surgery. Multiple, staged surgeries are not exclusionary
  • 18 years of age or older
  • The subject must in the investigator's opinion, be psychosocially, mentally, and physically able to fully comply with this protocol including the required follow-up visits, the filling out of required forms, and have the ability to understand and give written informed consent

Exclusion Criteria

  • Patient is a prisoner
  • Patient is not English speaking
  • Patient is not expected to survive until the 2-year follow-up

Outcomes

Primary Outcomes

PROMIS-29 quality of life outcome measures for patients undergoing endoscopic endonasal surgeries.

Time Frame: 24-months post-operatively

This study aims to better understand the long-term overall quality of life of patients undergoing endoscopic endonasal surgery using modern sinonasal reconstruction techniques. The PROMIS-29 metric, an overall quality of life metric, will be used to better understand quality of life for patients undergoing this procedure.

Secondary Outcomes

  • ASK Nasal-12 questionnaire used to measure normal time of healing for patients undergoing endoscopic endonasal surgery(24 months post-operatively)
  • Number of patients with long-term quality of life risk factors using PROMIS-29(24 months post-operatively)
  • Number of patients with long-term procedural comorbidities using ASK-Nasal 12.(24 months post-operatively)

Study Sites (1)

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