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| Sponsor: | National Heart, Lung, and Blood Institute (NHLBI) |
|---|---|
| Information provided by: | National Institutes of Health Clinical Center (CC) |
| ClinicalTrials.gov Identifier: | NCT00001621 |
Purpose
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.
| Condition |
|---|
|
Lung Disease |
| Study Type: | Observational |
| Official Title: | Evaluation and Treatment of Pulmonary Patients Not Participating in Research (Training Protocol) |
| Estimated Enrollment: | 99999999 |
| Study Start Date: | January 1997 |
The professional staff in the Cardiovascular and Pulmonary Branch (CPB) needs to maintain their clinical skills and to enhance their clinical knowledge. The purpose of this protocol is to permit CPB staff to evaluate and treat patients with pulmonary disease who do not meet the criteria for existing research protocols.
Eligibility| Ages Eligible for Study: | 8 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Patients 8 years old and older with signs or symptoms of pulmonary disease of medical interest to the professional staff of CPB 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.
Contacts and Locations| 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, Maryland | |
| National Institutes of Health Clinical Center, 9000 Rockville Pike | Recruiting |
| Bethesda, Maryland, United States, 20892 | |
| Sub-Investigator: Patient Recruitment and Public Liaison Office (PRPL) For more information at the NIH Clinical Center contact | |
More Information
| ClinicalTrials.gov Identifier: | NCT00001621 History of Changes |
| Other Study ID Numbers: | 970061, 97-H-0061 |
| Study First Received: | November 3, 1999 |
| Last Updated: | December 23, 2011 |
| Health Authority: | United States: Federal Government |
|
Teaching Pulmonary Disease Routine Testing Medically Indicated Pulmonary Function Test |
|
Lung Diseases Respiratory Tract Diseases |
