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Evaluation and Treatment of Patients With Lung Disease Not Participating in Research
This study is currently recruiting participants.
Study NCT00001621   Information provided by National Institutes of Health Clinical Center (CC)
First Received: November 3, 1999   Last Updated: September 19, 2009   History of Changes

November 3, 1999
September 19, 2009
January 1997
November 2001   (final data collection date for primary outcome measure)
 
To evaluate the feasibility of using G-CSF mobilized donor blood to transplant a predetermined dose of stem cells and T lymphocytes to recipients with hematologic malignacies.
Complete list of historical versions of study NCT00001621 on ClinicalTrials.gov Archive Site
 
 
 
Evaluation and Treatment of Patients With Lung Disease Not Participating in Research
Evaluation and Treatment of Pulmonary Patients Not Participating in Research (Training Protocol)

This study was developed in order for the professional-staff at the Pulmonary-Critical Care Medical Branch (PCCMB) of the National Heart, Lung, and Blood Institute to maintain their skills and increase their understanding of lung diseases.

The study will permit PCCMB staff members to evaluate and treat patients with lung disease who do not meet the criteria for other research studies.

The professional staff in theTranslational Medicine Branch (TMB) and Pulmonary and Vascular Medicine Branch (PVMB) needs to maintain their clinical skills to enhance their clinical knowledge. The purpose of this protocol is to permit TMB and PVMB staff to evaluate and treat patients with pulmonary disease who do not meet the criteria for existing research protocols.

 
Observational
 
Lung Disease
 
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
99999999
 
November 2001   (final data collection date for primary outcome measure)
  • INCLUSION CRITERIA:

Patients 8 years old and older with signs or symptoms of pulmonary disease of medical interest to the professional staff of PCCMB will be eligible for participation in this protocol. Children under the age of 18 who need medically indicated procedures will not be assented unless the child's dissent will be honored. Only standard diagnostic procedures and conventional therapy will be performed. Patients will not be subjected to any research procedures. This protocol does not commit the NIH to medical or surgical treatment of protocol participants after discharge. Patients will be discharged to the referring physician.

Consenting to pregnancy testing in minors of childbearing age:

We will inform the minor during the assent process that for safety, we need to do a pregnancy test. She will also be told that if it is positive, we will counsel her and help her tell her parents. If the minor does not want to proceed she will be advised not to sign assent and her enrollment on this training protocol will end.

EXCLUSION CRITERIA:

Patients without symptoms of pulmonary disease will be excluded from this protocol.

Both
8 Years and older
No
Contact: Patient Recruitment and Public Liaison Office (800) 411-1222 prpl@mail.cc.nih.gov
Contact: Mary Haughey, R.N. (301) 496-3632 mhaughey@nhlbi.nih.gov
United States
 
NCT00001621
 
970061, 97-H-0061
National Heart, Lung, and Blood Institute (NHLBI)
 
 
National Institutes of Health Clinical Center (CC)
July 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP