Evaluation of the Prevalence of Pulmonary Hypertension in Adult Patients With Sickle Cell Disease

NCT00434902 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 700

Last updated 2012-12-19

No results posted yet for this study

Summary

Recent data show that pulmonary hypertension (PH), defined by a tricuspid regurgitation jet (TRJ) velocity \> or equal at 2.5m/s on Doppler echocardiography, is present in about 30% of adults with sickle cell disease (SCD) and is associated with poor prognosis. However in SCD the occurrence of PH (defined by mean pulmonary arterial pressure (mPAP)\> or equal at 25 mmHg) is related to at least 3 mechanisms: PH due to hyperkinetic state with high cardiac output (CO) but normal pulmonary vascular resistance (PVR \<160 dynes), or postcapillary PH (pulmonary capillary wedge pressure PCWP \>15 mmHg), or precapillary pulmonary arterial hypertension (PAH) defined by mPAP \> or equal at 25 mmHg, PCWP\< or equal at 15 mmHg and PVR \> or equal at 160 dynes.The aim of this study is to evaluate in a French population of adults with sickle cell disease the characteristics, prevalence and prognosis of pulmonary hypertension.

Conditions

Sponsors & Collaborators

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Gerald SIMONNEAU, MD · Hôpital Antoine Béclère, CLAMART

  • Frederic Galacteros, MD · Hôpital Henri Mondor, Creteil

  • Serge ADNOT, MD · Hôpital Henri Mondor, CRETEIL

  • Bernard MAITRE, MD · Hopital Henri Mondor, CRETEIL

  • Marc HUMBERT, MD · Hôpîtal Antoine Béclere, CLAMART

  • Robert GIROT, MD · Hôpital Tenon, PARIS

  • François LIONNET, MD · Hôpital TENON, PARIS

  • Françoise DRISS, MD · Hôpital Bicêtre, KREMLIN BICETRE

  • Olivier LAMBOTTE, MD · Hôpital Bicêtre, KREMLIN BICETRE

  • Jocelyn INAMO, MD · CHU Fort de France

  • Gylna LOKO, MD · CHU Fort de France

  • Olivier SITBON, MD · Hôpital Antoine Béclère, CLAMART

  • Xavier Jaïs, MD · Hôpital Antoine Béclère, CLAMART

  • Anoosha Habibi, MD · Hôpital Henri Mondor, CRETEIL

  • Dora Bachir, MD · Hôpital Henri Mondor, CRETEIL

  • Laurent SAVALE, MD · Hopital Henri Mondor, CRETEIL

  • Saadia Eddahibi, MD · Hôpital Henri Mondor, CRETEIL

  • Gilles Garcia, MD · Hopital Antoine Béclère, CLAMART

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-02-28
Primary Completion
2009-03-31
Completion
2012-12-31

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00434902 on ClinicalTrials.gov