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Contrast-Enhanced US of Spleen, Liver and Kidney

Contrast-Enhanced US of Spleen, Liver and Kidney in Patients With Acute Infection (Malaria and Other Infectious Diseases: a Functional Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00190281
Enrollment
53
Registered
2005-09-19
Start date
2005-08-31
Completion date
Unknown
Last updated
2005-12-13

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

Conditions

Bacterial Infections, Malaria, Pyelonephritis

Keywords

FUNCTIONAL STUDY, CONTRAST-ENHANCED US, PERFUSION

Brief summary

To evaluate the changes in the microcirculation of the liver, kidney and spleen during acute infection in patients with malaria (cohorts 1 and 3) and other infectious diseases such as acute pyelonephritis at day 0 (within 8 hours of the treatment start), day 2 to 4 and day 28-32, using functional US with continuous infusion of a contrast agent (SonoVue, Bracco, Italy). Study hypothesis: malaria patients should exhibit a different pattern of enhancement, particularly when quantitative measurements of the SU signals is performed with destruction reperfusion kinetics.

Detailed description

To evaluate the changes in the microcirculation of the liver, kidney and spleen during acute infection in patients with malaria (cohorts 1 and 3) and other infectious diseases such as acute pyelonephritis at day 0 (within 8 hours of the treatment start), day 2 to 4 and day 28-32, using functional US with continuous infusion of a contrast agent (SonoVue, Bracco, Italy). Three cohortes will be studied: cohorte 1 infection at Plasmodium falciparum (24 patients), cohorte 3 infection at Plasmodium vivax, ovale or malariae (5 patients) and cohorte 2 other infectious diseases such as acute pyelonephritis (24 patients). Study hypothesis: malaria patients should exhibit a different pattern of enhancement, particularly when quantitative measurements of the SU signals is performed with destruction reperfusion kinetics.

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
DEFINED_POPULATION
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Social security number * Age over 18 * acute malaria infection or other infectious diseases * Inpatients * Signed informed consent form

Exclusion criteria

* Pregnancy * Criteria of bad tolerance of infection * Treatment started for more than 8 hours * Lack of cooperation * History of splenectomy, hematological disease, cirrhosis with portal hypertension, splenomegaly * Medical treatment with beta blocker, diuretic, immunodepression drugs

Countries

France

Contacts

Primary ContactOlivier Lortholary, MD PhD
olivier.lortholary@nck.ap-hop-paris.fr33-1-44-49-41-42

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026