Pulmonary Hypertension Prevention in Hemodialysis
This study is not yet open for participant recruitment.
Verified April 2011 by The Baruch Padeh Medical Center, Poriya
Sponsor:
The Baruch Padeh Medical Center, Poriya
Information provided by:
The Baruch Padeh Medical Center, Poriya
ClinicalTrials.gov Identifier:
NCT01350687
First received: May 8, 2011
Last updated: May 9, 2011
Last verified: April 2011
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
Pulmonary hypertension is a new complication described in hemodialysis patients. in the last year these patients were treated by calcium carbonate orally to control serum phosphor. Calcium phosphor deposits in pulmonary artery can explain this phenomena. The investigators want to investigate the new phosphor non calcium containing agents in hemodialysis patients and to measure the pulmonary pressure.
| Condition |
|---|
|
Chronic Kidney Disease |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | New Phosphore Binders in Prevention of Pulmonary Hypertension |
Resource links provided by NLM:
MedlinePlus related topics:
Calcium
Chronic Kidney Disease
Dialysis
High Blood Pressure
Pulmonary Hypertension
U.S. FDA Resources
Further study details as provided by The Baruch Padeh Medical Center, Poriya:
| Estimated Enrollment: | 40 |
| Study Start Date: | June 2011 |
| Estimated Study Completion Date: | June 2014 |
| Estimated Primary Completion Date: | June 2013 (Final data collection date for primary outcome measure) |
The investigators will measure pulmonary blood pressure before and after treatment with new phosphor binders, non calcium containing.
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
40 patients on hemodialysis treated with Phosphore biders, non-calcium containig.
Criteria
Inclusion Criteria:
- Hemodialysis Patients without fistula
Exclusion Criteria:
- Heart Disease
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01350687
Locations
| Israel | |
| Poria Medical Center | Not yet recruiting |
| Tiberias, Israel | |
| Contact: Farid Nakhoul, Prof 97246652587 fnakhoul@poria.health.gov.il | |
| Principal Investigator: Farid Nakhoul, Prof | |
Sponsors and Collaborators
The Baruch Padeh Medical Center, Poriya
Investigators
| Study Chair: | Farid Nakhoul, Prof. | Poria medical Center |
More Information
No publications provided
| Responsible Party: | Avi On, Poria Medical Center |
| ClinicalTrials.gov Identifier: | NCT01350687 History of Changes |
| Other Study ID Numbers: | farid.CTIL |
| Study First Received: | May 8, 2011 |
| Last Updated: | May 9, 2011 |
| Health Authority: | Israel: The Israel National Institute for Health Policy Research and Health Services Research |
Keywords provided by The Baruch Padeh Medical Center, Poriya:
|
Calcium Phosphore Renagel |
Additional relevant MeSH terms:
|
Hypertension Hypertension, Pulmonary Kidney Diseases Renal Insufficiency, Chronic Kidney Failure, Chronic Vascular Diseases |
Cardiovascular Diseases Lung Diseases Respiratory Tract Diseases Urologic Diseases Renal Insufficiency |
ClinicalTrials.gov processed this record on May 16, 2013