ClinicalTrials.gg
CompletedNCT00929565Updated Apr 9, 2012

Urokinase Like Plasminogen Activator Levels in Patients Undergoing Bronchoscopy

An observational study in Hemoptysis, sponsored by University of Oklahoma. Completed at 1 site in United States. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2012-04-09.

Sponsored by University of Oklahoma · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
10
Ages
18 Years to 80 Years
Sex
All
01

Study summary

Some of the risk factors for bleeding following bronchoscopy is having a malignancy or an immunocompromised state. The etiology of this remains uncertain. The investigators suspect that individuals with malignancy have abnormalities involving certain factors that influence the coagulation pathway.

The investigators plan to measure these factors prior to and after bronchoscopy.

Read the detailed description

This is a prospective observational study looking at some coagulation factors in individuals with lung cancer. We are looking at BAL and plasma. We would like to see if there is a difference in the levels and if this is the reason behind the higher incidence of hemoptysis in patients with lung cancer.

02

Conditions studied

  • Hemoptysis

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Keywords

  • hemoptysis
03

In context

Hemoptysis

37 studies on the registry are indexed under Hemoptysis; 6 are open to participants now.

This study's enrollment of 10 is below the median of 176 across 15 observational studies indexed under Hemoptysis.

Browse Hemoptysis studies →

Lead sponsor

University of Oklahoma is the lead sponsor of 432 studies on the registry; 100 are open to participants now.

Of its 42 completed or terminated interventional studies of FDA-regulated products, 16 (38%) have results posted.

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

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients from the VAMC in Oklahoma city

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Any patient scheduled to undergo bronchoscopy

Exclusion criteria

Exclusion Criteria:

  • Patients with evidence of coagulopathy either iatrogenic or the result of disease process - coagulopathy defined as elevated , activated partial thromboplastin time or count less than 100,000
  • Patients not scheduled to undergo bronchoalveolar lavage (BAL)
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

INR, PT and aPTT (clotting tests)

Blood tests of how long blood takes to clot. The INR is the prothrombin time (PT) put on a common scale; about 1 is usual for someone not taking a blood thinner.

Criteria often make an exception for people on a blood thinner such as warfarin, whose INR is raised on purpose.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
10 participants (actual)

Groups and cohorts

  • Lung cancer

    Comparison between individuals with and without pulmonary malignancy

06

What researchers measure

Secondary outcomes

  1. Volume of blood loss during the procedure

    Time frame: 1 day

07

Study locations

1 site
  • VA Medical Center
    Oklahoma City, Oklahoma 73104, United States
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jun 2009, a primary completion of Jun 2010 and a completion of Oct 2011. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 24, 2009
First posted
Jun 29, 2009
Start
Jun 2009
Primary completionActual
Jun 2010
CompletionActual
Oct 2011
Last update
Apr 9, 2012
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 9, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00929565
Responsible party
Gary Kinasewitz (Principal Investigator, University of Oklahoma) — Principal investigator
First posted
Jun 29, 2009
Start date
Jun 2009
Primary completion
Jun 2010
Completion
Oct 2011
Last update
Apr 9, 2012

Study contacts

Jijo John, MD
principal investigator · University of Oklahoma

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2012. You cannot join it, but the record below documents what was studied.

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