Adherence in Global Airways - Steroid Intake and Effects on Chronic Rhinosinosinutis

NCT ID: NCT05843019

Last Updated: 2023-06-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-04-12

Study Completion Date

2025-12-31

Brief Summary

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The purpose of this study is to investigate the relationship between long-term use of systemic steroids in patients with upper and lower respiratory tract diseases and their own production of cortisol (cross-sectional), as well as whether those with low cortisol levels have an impact on bone density. As patients with CRSwNP have a high use of steroids, they routinely undergo a DEXA scan at the Respiratory Clinic, Department of Ear-Nose-Throat Surgery and Audiology (ENT) - Rigshospitalet (RH) to examine whether their bone density and structure are affected. The scan will be included as a clinical secondary outcome to assess whether systemic steroid use has an impact on this.

The purpose of the study is therefore to compare steroid intake, baseline P-cortisol, the body's response to ACTH (measured by cortisol levels after the test), and bone density in patients with chronic sinusitis (CRS) with and without asthma in an unselected population at the Respiratory Clinic (cross-sectional). In addition, at the 4-month follow-up (exploratory follow-up, pilot project), it will be investigated whether good adherence (\>80%) to inhalation therapy (nasal steroid and lung steroid) and additional treatment with biologicals has a negative effect on the body's own production of P-cortisol.

Detailed Description

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Conditions

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Chronic Rhinosinusitis Without Nasal Polyps Asthma Chronic Rhinosinusitis With Nasal Polyps Steroid-Induced Osteopenia (Diagnosis) Steroid-Induced Diabetes Steroid-Induced Hyperglycemia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Cross sectional

The patients in the cross sectional study will have done a synactenstest to investigate how their own product of kortisol os after longterm use of systemic steroids.

The group consists of patients referred to the Respiratory Clinic, ENT, RH, for evaluation of CRS/CRSwNP/CRSnNP and with or without asthma for biological treatment. They are classified according to the type of inflammation they have (type-2 or non-type-2), whether they have CRSwNP or CRSsNP, their adherence, comorbidity with asthma, and finally the severity of the disease. All patients are given standard questionnaires to assess CRS/CRSwNP/CRSnNP and asthma (STARR-15, SNOT22, ACQ, ACT, MARS-5-L/N, Fosterscore - routine questionnaires for all patients in the Respiratory Clinic).

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Diagnosed with chronic rhinosinusitis (CRS)
* possibly asthma
* Aged over 18 years


* Diagnosed with CRS and possibly asthma
* Age over 18 years
* Low adherence: Foster score, i.e. the number of treatments taken compared to prescribed \< 80% (4 weeks out of 16 weeks) and/or measured on MARS-5 L/N ≤35 at the first visit (corresponding to less than 80%). If the patient does not have asthma, it is MARS-5N ≤ 19
* If asthma: ACQ ≥1.2 or ACT ≤ 17 (partly uncontrolled asthma)
* SNOT-22 score ≥35 (partly uncontrolled CRS)
* Participation in the cross-sectional study at the initial visit to the Respiratory Clinic

Exclusion Criteria

* Unable to read or speak Danish
* Presence of severe psychiatric comorbidities
* Patients who have never taken systemic steroids
* Inability to participate or comply with local treatment according to the investigators' assessment
* Does not provide consent for lookup in FMK-online



Adherence:

* Foster score \>80% and/or on MARS-5-L/N \>35 points at the first visit
* Cannot read or speak Danish
* Severe psychiatric comorbidities
* Patients who have never taken systemic steroids
* After investigators' experience, will not be able to participate or comply with local treatment
* Does not give permission to look up data in FMK-online.
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Christiane Haase

OTHER

Sponsor Role lead

Responsible Party

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Christiane Haase

Clinical nurse specialist and Phd-student

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Department of Otorhinolaryngology, Head and Neck Surgery & Audiology

Copenhagen, Denamrk, Denmark

Site Status RECRUITING

Countries

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Denmark

Central Contacts

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Christiane PS Haase

Role: CONTACT

+4535459565

Vibeke P Backer

Role: CONTACT

+4535456033

Facility Contacts

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Christiane PS Haase

Role: primary

+4535459565

Vibeke P Backer

Role: backup

+4535456033

Provided Documents

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Document Type: Study Protocol and Informed Consent Form

View Document

Other Identifiers

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2022-ENT-steroids

Identifier Type: -

Identifier Source: org_study_id

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