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Investigation of relationship between the pathogenesis of pulmonary hypertension and dysbiosis

Investigation of relationship between the pathogenesis of pulmonary hypertension and dysbiosis - Pulmonary hypertension and dysbiosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000025652
Enrollment
40
Registered
2017-01-12
Start date
2018-05-22
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

Pulmonary arterial hypertension Chronic thromboembolic pulmonary hyperetension

Interventions

None listed

Sponsors

Graduated School of Medicine, Chiba University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who diagnosed as PAH or CTEPH in our institution.Inclusion criteia of patients were as follows. 1) adult patients (>20years old) 2) Mean pulmonary arterial pressure was above 25mmHg 3) Patients give written informed consents Healthy control subjects are recruited from staffs of our institution. Inclusion criteria of healthy control subjects are as follows. 1) adult patients (>20years old) 2) Patients give written informed consents

Exclusion criteria

Exclusion criteria: Exclusion criteria of PH patients or healthycontrol subjects are as follows. 1) uncontrolled diabetes mellitus 2) history of myocardial infarction 3) history of unstable angina pectoris 4) subjects with severe liver dysfunction (AST or ALT >150) 5) subjects with severe renal dysfunction (BUN >30mg/dl or Creatinine >2.0mg/dl) 6) pregnant female subjects 7) breast feeding female subjects 8) Exclusion by Investigators in safety

Design outcomes

Primary

MeasureTime frame
Following endpoints were evaluated at diagnosis, 6, 12,24,36 months after starting treatments. 1) The composition of intestinal flora by 16S rRNA analysis 2) Functional analysis by meta-genome analysis

Secondary

MeasureTime frame
Following endpoints were evaluated at diagnosis, 6, 12,24,36 months after starting treatments. 1) Right heart categorization 2) echocardiography 3) blood examination (BNP, UA, CRP) 4) fecal biochemistry (butyric acid, lactic acid) 5) analysis of oral flora 6) Physical activity

Countries

Japan

Contacts

Public ContactTakayuki Jujo

Graduated School of Medicine, Chiba University Department of Advanced Medicine in Pulmonary Hypertension

naikamo_resp19184@yahoo.co.jp043-222-7171

Outcome results

None listed

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