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Completed

NCT Number: NCT06589492

Comparison of Serum SIRT-1 and MMP-9 Levels of Patients With Bronchiectasis and Healthy Controls

The purpose of this a cross-sectinol study is to measure the levels of MMP-9 and SIRT-1 levels in patients with bronchiectasis and healthy controls. The aim is to compare the serum levels of these molecules between patients and controls.

* Is the MMP-9 level increasing or decreasing? * Is the SIRT-1 level increasing or decreasing in patients? * Is the disease related to age and gender? Participants will only have one 5 ml blood sample drawn when they visit the chest illness clinic. Molecule levels will be measured in this blood's serum.

The patient group participants will be scanned once with high-resolution chest CT.

Apart from this, comparisons will be made using the age and gender information of the participants.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cumhuriyet University

Sivas, Si̇vas Centre, Turkey (Türkiye)

About this study

In the overall study population of 60 subjects who applied to the Sivas Cumhuriyet University Faculty of Medicine Research and Practice Hospital Chest Diseases Clinic. The study population was selected regardless of age and gender. Participants selected bronchiectasis patients (n=30) who had symptoms (cough, sputum production) and had their diagnosis confirmed by a chest high-resolution CT scan within the previous year. The study excluded individuals with bronchiectasis not associated with cystic fibrosis and who had a worsening episode (according to the 2017 European Respiratory Society expert consensus criteria) (16) or had taken antibiotics during the previous four weeks. The study enrolled healthy controls (n=30) through advertisements who had acceptable chest X-ray and spirometry results and no lower airway symptoms or serious systemic disorders. The study eliminated individuals who were pregnant or nursing, as well as those with low comprehension. SIRT-1 and MMP-9 levels in the serum of the study group were determined by the ELISA method.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Bronchiectasis patients who were symptoms (cough, sputum production)
  • Individuals whose diagnosis was confirmed by a high-resolution chest CT scan taken within the previous year

Exclusion criteria

  • Individuals with bronchiectasis associated with cystic fibrosis and who had a worsening episode
  • individuals who were pregnant or nursing
  • those with low comprehension
  • taken antibiotics during the previous four weeks

Treatment and study plan

Measurement of MMP-9 and SIRT-1 levels in blood serum

Diagnostic Test

Measurement of MMP-9 and SIRT-1 levels in blood serum, Collection of 5 ml Blood samples

Primary outcomes

  1. MMP-9 and SIRT-1 levels (ng/mL) mesurment in the blood serum to compare between patient and control.

    Time frame: not measured in time frame. general (1. day)

    MMP-9 and SIRT-1 levels mesured in the blood serum. The most common side effect when blood is taken from the patient is slight bruising and swelling in the arm due to needle sticking. There will be no other serious side effects.

Sponsors and collaborators

Lead sponsor

Cumhuriyet University

Other

Registry information

Official study title

A Cross-sectional Study on the Comparison of Serum SIRT-1 and MMP-9 Levels of Patients With Bronchiectasis and Healthy Controls

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Sep 19, 2024
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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