Impact of Capillaroscopy in the Investigation of Diffuse Interstitial Pneumonias (CAPID)

The investigators hypothesize that in patients with a new diagnosis of Pulmonary Interstitial Disease (PID), adding capillaroscopy to standard care increases the proportion of patients receiving a diagnosis of PID-Connective Tissue Disease (PID-CTD) within the first three months of follow-up, thereby reducing the time to diagnosis and facilitating the implementation of appropriate treatment as quickly as possible. Therefore, To confirm this hypothesis, it is necessary to know the characteristics of capillaroscopy in patients with a new diagnosis of PID.

Study Overview

• Status: Recruiting
• Conditions: Connective Tissue Diseases; Interstitial Lung Disease
• Intervention / Treatment: Diagnostic test: capillaroscopy

Detailed Description

Diffuse interstitial lung diseases (DILD) are a group of diseases characterized by inflammation and fibrosis of the lung tissue, with more than 200 identified causes, approximately 20% of which are related to autoimmune diseases such as connective tissue disorders (e.g., scleroderma, lupus). Pulmonary involvement may precede the diagnosis of connective tissue disease, making diagnosis difficult. Capillaroscopy, a non-invasive and reproducible test, is used to detect microvascular abnormalities, especially in scleroderma spectrum diseases, but its precise role in the evaluation of PID is still poorly defined. Studies show that PIDs associated with autoimmunity are more likely to present with capillaroscopic abnormalities. However, current recommendations on the investigation of PIDs do not clearly specify the use of capillaroscopy, and there are no studies establishing its value in systematic screening of all patients with PID. Thus the investigators aim to describe the characteristics of capillaroscopy in patients with a new diagnosis of PID.

The project will be offered to eligible patients for whom a PID has been identified. A review of the medical record information will then be carried out, with additional tests performed as necessary to identify the etiology associated with this IDP. The compilation of information, and especially the performance of additional tests (beyond normal care), is typically completed within three months. In the meantime, and particularly in the first month after signing the consent form, the patient will undergo a capillaroscopy and complete the patient questionnaire. After three months, once all additional tests have been performed and the results compiled, the pulmonologist completes the questionnaire to identify the most likely etiology of the patient's PID. All tests, except for capillaroscopy, are performed as part of routine care.

• Study Type: Interventional
• Enrollment (Estimated): 48
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Thomas BARNETCHE, PhD; Email: thomas.barnetche@chu-bordeaux.fr
• Study Contact Backup: Name: Marie-Elise TRUCHETET, MD, PhD; Phone Number: +33 05.56.79.55.56; Email: marie-elise.truchetet@chu-bordeaux.fr

Study Locations

• France
  • Bordeaux, France
    • Recruiting
    • CHU de Bordeaux - service de rhumatologie
    • Principal Investigator: Marie-Elise TRUCHETET, Prof
    • Contact: Marie-Elise TRUCHETET, MD, PhD; Phone Number: +33 05.56.79.55.56; Email: marie-elise.truchetet@chu-bordeaux.fr
    • Sub-Investigator: Elodie BLANCHARD, MD
    • Contact: Thomas BARNETCHE, PhD; Email: thomas.barnetche@chu-bordeaux.fr

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Male or female over 18 years of age;
• Have received a new diagnosis of PID within the last six months, confirmed by a pulmonologist;
• Have undergone some specific tests within the last six months (Chest CT scan, respiratory function tests (plethysmography and CO transfer capacity measurement, immunological assessment including: screening for FAN, FR, and anti-CCP);
• French-speaking patient with no comprehension difficulties;
• Person affiliated with or beneficiary of a social security system;
• Free, informed, and written consent signed by the participant and the investigator (no later than the day of inclusion and before any examination required by the research).

Exclusion Criteria:

• Have previously undergone a capillaroscopy, regardless of the reason;
• Have a diagnosis or high suspicion of connective tissue disease based on initial clinical and paraclinical evaluation;
• Have already started one of the following treatments for pulmonary involvement: systemic corticosteroids, immunosuppressive therapy, antifibrotic therapy;
• Pregnant or breastfeeding women;
• Patients covered by Articles L 1121-5 to L 1121-8 (persons deprived of their liberty by judicial or administrative decision, minors, adults subject to legal protection measures, or persons unable to give their consent).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Diagnostic
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Diffuse interstitial lung diseases (DILD)	Diagnostic test: capillaroscopy; Capillaroscopy will be performed during a specific consultation. During this examination, a device called a "video capillaroscope" is used to magnify and visualize the capillaries located at the base of the nail. The examination lasts approximately twenty minutes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Proportion of capillaroscopy abnormalities according to the classification proposed by the EULAR Study Group on Microcirculation in Rheumatic Diseases	At baseline (Day 0)

Secondary Outcome Measures

Outcome Measure	Time Frame
Description of the criteria that may influence the results of capillary examination: proportion of smoking status categories (active smoker/non-smoker/former smoker) and number of cigarettes per day for active smokers	At baseline (Day 0)
Description of the criteria that may influence the results of capillary examination: number of cigarettes per day for active smokers	At baseline (Day 0)
Description of the criteria that may influence the results of capillary examination: proportion of patients who consume alcohol	At baseline (Day 0)
Description of the criteria that may influence the results of capillary examination: average number of standard drinks for active consumers.	At baseline (Day 0)

Collaborators and Investigators

• Sponsor: University Hospital, Bordeaux
• Investigators: Principal Investigator: Marie-Elise TRUCHETET, MD, PhD, University Hospital, Bordeaux

Study record dates

Study Major Dates

• Study Start (Actual): March 16, 2026
• Primary Completion (Estimated): March 1, 2027
• Study Completion (Estimated): March 1, 2027

Study Registration Dates

• First Submitted: December 2, 2025
• First Submitted That Met QC Criteria: December 2, 2025
• First Posted (Actual): December 15, 2025

Study Record Updates

• Last Update Posted (Actual): March 20, 2026
• Last Update Submitted That Met QC Criteria: March 17, 2026
• Last Verified: March 1, 2026

More Information

Terms related to this study

• Keywords: diagnosis; Connective Tissue Disease; capillaroscopy; Pulmonary Interstitial Disease
• Additional Relevant MeSH Terms: Pathologic Processes; Respiratory Tract Diseases; Lung Diseases; Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Disease; Lung Diseases, Interstitial; Connective Tissue Diseases; Investigative Techniques; Diagnostic Techniques and Procedures; Diagnosis; Diagnostic Imaging; Diagnostic Techniques, Cardiovascular; Microscopy; Intravital Microscopy; Microscopic Angioscopy
• Other Study ID Numbers: CHUBX 2025/086

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No