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Status unknownNCT00538044Updated Oct 2, 2007

Simvatstatin Used to Treat Pulmonary Hypertension

A Phase 1 interventional study of simvastatin in Hypertension, Pulmonary, sponsored by Capital Medical University. Status unknown at 1 site in China. Open to participants aged 12 Years to 70 Years. Per ClinicalTrials.gov, last updated 2007-10-02.

Sponsored by Capital Medical University · Phase 1, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Sep 2007), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 1
Study type
Interventional
Allocation
Randomized
Ages
12 Years to 70 Years
Sex
All
01

Study summary

we try to use simvastatin in the treatment of advanced pulmoary hypertension secondary to congenital heart disease or chronic pulmonary embolism before and after the operation.

Read the detailed description

advanced pulmonary hypertension is refractory to the medication in use nowaday, especially pulmonary hypertension secondary to congenital heart disease or chronic pulmonary embolism.It is revealed that statins may intefere the pathogenisis of the pulmonary hypertension in many key poing, such as improving apotosis or inhiting the proliferation of pulmonary vascular smooth muscle cell. so we try to use simvastatin in the treatment of advanced pulmoary hypertension secondary to congenital heart disease or chronic pulmonary embolism before and after the operation.

02

Conditions studied

  • Hypertension, Pulmonary

Keywords

  • pulmonary hypertension
  • simvastatin
  • advanced pulmonary hypertension secondary to congenital heart disease
  • advanced pulmonary hypertension secondary to chronic pulmonary embolism
03

In context

Hypertension, Pulmonary

1,105 studies on the registry are indexed under Hypertension, Pulmonary; 234 are open to participants now.

Browse Hypertension, Pulmonary studies →

Lead sponsor

Capital Medical University is the lead sponsor of 283 studies on the registry; 92 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • pasp>50mmHg

Exclusion criteria

Exclusion Criteria:

  • pasp\<50mmhg
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)

Study arms

  • Experimental
    1simvastatin group

    before the operation, the patient start the simvastatin medication on the dosage of 40mg per day

    Drug: simvastatin

  • No intervention
    2contral group

    just do routin operation with no use of simvastatin, other medication is exact the same as the simvastatin group

Interventions

  • Drugsimvastatin

    medication with simvastation on the dosage of 40mg per day before the operation and all the time after the operation

06

What researchers measure

Primary outcomes

  1. the simvastatin can alleviate pulmonary hypertension

  2. pulmonary pressure

Secondary outcomes

  1. simvastatin can highten the perioperative and long term survaval rate and the living quality

07

Study locations

1 site
  • Beijing Anzhen Hospital
    Beijing, 100029, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 2, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00538044
Lead sponsor
Capital Medical University
First posted
Oct 2, 2007
Start date
Jan 2009
Completion
Jan 2012 (estimated)
Last update
Oct 2, 2007

Study contacts

Huili Gan, MD,Ph.D.
Contact
ganhuili@hotmail.com
13001277863
Huili Gan, MD,Ph.D.
study chair · Beijing Anzehn Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2007. You cannot join it, but the record below documents what was studied.

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