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Perioperative Use of Inhaled and Intravenous Iloprost in Patients with Pulmonary Hypertension during Non-cardiac Surgery

Iloprost in Patients with Pulmonary Hypertension during Non-cardiac Surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-12002826
Enrollment
Unknown
Registered
2012-12-21
Start date
2008-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Patients with Pulmonary Hypertension

Interventions

treatment group:Iloprost Inhalation

Sponsors

Beijing Shijitan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Severe pulmonary hypertension patients undergoning selective non-cardiac operation; (2) mPAP>25mmHg, PCWP3 wood unit; (3) excluded pulmonary arterial hypertension secondary to pulmonary diseases; (4) 6MWD between 150m and 450m; (5) WHO pulmonary hypertension functional Class II - III; (6) acquired informed consent.

Exclusion criteria

Exclusion criteria: (1) denied informed consent and no cooperative patients; (2) with sever hepatic, renal and central nervous system diseases; (3) with unstable angina or myocardial infarction, stoke, and fatal arrhythemia within 6 months.

Design outcomes

Primary

MeasureTime frame
pulmonary hemodynamic indeces;

Countries

China

Contacts

Public ContactLei Pan
leipan61@yahoo.com.cn+86 10 63926750

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026