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The retrospective study of treatment by thrombomodulin for acute exacerbations of idiopathic pulmonary fibrosis, acute respiratory distress sydmrome

The retrospective study of treatment by thrombomodulin for acute exacerbations of idiopathic pulmonary fibrosis, acute respiratory distress sydmrome - The treatment of thrombomodulin for acute respiratory failure

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000012590
Enrollment
50
Registered
2014-01-01
Start date
2010-04-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acute exacerbations of idiopathic pulmonary fibrosis, acute respiratory distress syndrome

Interventions

Thrombomodulin

Sponsors

Chiba University
Lead Sponsor
ShinonoiGeneral Hospital First Department of Internal Medicine, Shinshu University School of Medicine
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The diagnosis of AE-IPF was based on the criteria, which state that all of the following three conditions must be satisfied during the course of IPF with an unexplained worsening of dyspnea within one month: (1) increased dyspnea, (2) new HRCT appearance, (3) greater than 10-mmHg decreases in oxygen partial pressure (PaO2) in the resting arterial blood compared to previous measurements. The typical HRCT appearance of AE-IPF involved ground glass opacity and/or consolidation as a new appearance on honeycombing. The criteria for the diagnosis of ARDS, as set by the Berlin Definition

Exclusion criteria

Exclusion criteria: The AE-IPF-patients were excluded if they had obvious signs of infection, preexisting pulmonary embolisms, left heart failure, pulmonary hypertension due to pulmonary thromboemboli or phlebitis based on the findings of color Doppler ultrasonography or enhanced HRCT. Patient or family refusal for invasive mechanical ventilation was an exclusionary criterion for endotracheal intubation. Such patients were excluded from this study.

Design outcomes

Primary

MeasureTime frame
The outcomes of patients included the 28-day mortality and in-hospital mortality after beginning treatment with rhTM were compared with those of untreated patients.

Secondary

MeasureTime frame
We investigated whether or not they showed any improvement in oxygenation (SpO2/FIO2) and intravascular coagulation disturbance (TAT, FDP) in the acute phase.

Countries

Japan

Contacts

Public ContactKenji Tsushima

Chiba University Department of Respirology, Graduate School of Medicine

tsushimakenji@yahoo.co.jp043-226-2800

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026