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Trauma Patients With Soft Tissue DefectsNCT00564109

Are the Pancreatic Serum Proteins Pancreatic Stone Protein (PSP) and Pancreatitis-Associated Protein (PAP) Predictive for the Development of Sepsis? Retrospective Study in Trauma Patients With Soft Tissue Defects.

An observational study of Trauma Patients With Soft Tissue Defects, run by University of Zurich at 1 site in Switzerland.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Retrospective analysis of PSP- and PAP-serum levels in trauma patients with soft tissue defects and possible correlation with the incidence and onset of infection and sepsis. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Trauma Patients With Soft Tissue Defects
What is being tested?
retrospective Observation
Type of treatment
Surgery or procedure
How many people
15 participants
Where
1 siteSwitzerland
Study dates
Aug 2005to Jan 2008
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Trauma patients

Who may be able to join

  • Trauma patients submitted to the university hospital Zurich, aged 18-65 with soft tissue defects

Who cannot join

  • Patients with known immunocompromising illnesses, drug abuse or infectious diseases.

Trial locations and contacts

1 site in 1 country.

01 Studienregister MasterAdmins contact

+41 (0)44 255 11 11

Switzerland1 site, 1 recruiting
  • Study site

    Zurich

    Recruiting

Other trials in Switzerland

About this study

Retrospective analysis of PSP- and PAP-serum levels in trauma patients with soft tissue defects and possible correlation with the incidence and onset of infection and sepsis.

Being tested
retrospective Observation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • retrospective ObservationProcedure or surgery

    retrospective Observation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Nov 2007 (estimated)
  2. Study startAug 2005
  3. Study completionJan 2008

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
15 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00564109
Sponsor's protocol ID
StV 10-2003
Status last verified
Nov 2007
First submitted
26 Nov 2007
Last updated
18 Mar 2008
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Trauma Patients With Soft Tissue Defects, run by University of Zurich at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 18 Mar 2008. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact 01 Studienregister MasterAdmins (+41 (0)44 255 11 11), or a site near the patient. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Mar 2008.

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