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NCT06976762Enrolling by invitation

Near-Infrared Spectroscopy Measurements in Chronic Obstructive Pulmonary Disease

Near-Infrared Spectroscopy Measurements in Patients With Chronic Obstructive Pulmonary Disease, and Chronic Renal Disease: An Observational Study

Source: ClinicalTrials.gov · Last updated 16 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Participants were selected based on three groups: healthy, chronic obstructive pulmonary disease, and chronic renal disease. NIRS was used to measure tissue oxygenation on the thenar region of the right hand. A pressure cuff was used to temporarily occlude arterial inflow, thus allowing the response to this to be assessed. The StO2 was plotted against time, and the following variables were calculated, the downslope, upslope, area under curve.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
140 (estimated)
First submitted
7 Dec 2024
Start date
1 May 2025
Primary completion date
30 May 2025
Lead sponsor
Tokat Gaziosmanpasa University
NCT number
NCT06976762

What you commit to

  • Study type: Observational
  • Planned participants: 140
  • From 1 May 2025 to the primary completion date, 30 May 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients were excluded from the study if they met any of the following criteria:
    • Acute Exacerbation: Evidence of an acute COPD exacerbation within four weeks prior to enrolment.
    • Other Respiratory Disorders: Coexistence of other chronic respiratory diseases such as asthma, interstitial lung disease, or bronchiectasis that might interfere with the assessment of COPD.
    • Renal Transplantation: History of kidney transplantation, as immunosuppressive therapy may affect disease progression and outcomes.
    • Uncontrolled Comorbidities: Presence of any uncontrolled comorbid conditions, including:
    • Cardiovascular instability or recent myocardial infarction (within six months).
    • Active malignancy (other than localized skin cancer).
    • Severe liver disease (e.g., cirrhosis with hepatic failure).
    • Pregnancy or Breastfeeding: Women who were pregnant or breastfeeding at the time of study enrolment.
    • Cognitive Impairment: Any condition that would impair the ability to provide informed consent or participate in study procedures, such as dementia or significant psychiatric disorders.

Who the study is looking for

  • To be eligible for the study, patients were required to meet all of the following criteria:
    • Age: Patients aged between 18 and 80 years.
    • COPD Diagnosis: A confirmed diagnosis of COPD according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria, including:
    • A post-bronchodilator forced expiratory volume in one second (FEV1) to forced vital capacity (FVC) ratio of \<0.70.
    • Renal Failure: Evidence of CKD, defined as:
    • An estimated glomerular filtration rate (eGFR) of \<60 mL/min/1.73 m² (Stages 3-5 CKD) on at least two occasions three months apart, or a history of renal replacement therapy.
    • Stable Medical Condition: Clinically stable COPD, with no exacerbations or hospital admissions within the preceding four weeks.

Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tokat Gaziosmanpaşa University
Coordinator of this site? Confirm its status
Tokat ProvinceTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.