Value of Amphotericin B Inhalation for Prophylaxis of Invasive Pulmonary Aspergillosis After Renal Transplantation
The recruitment status of this study is unknown because the information has not been verified recently.
Verified September 2009 by Capital Medical University.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
Capital Medical University
Information provided by:
Capital Medical University
ClinicalTrials.gov Identifier:
NCT00986713
First received: September 29, 2009
Last updated: NA
Last verified: September 2009
History: No changes posted
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Purpose
The purpose of this study is to determine whether inhalation with aerosolized amphoterin B 10mg/d is more effective than aerosolized amphoterin B 2mg/d to reduce the incidence of invasive pulmonary aspergillosis.
| Condition | Intervention | Phase |
|---|---|---|
|
Invasive Pulmonary Aspergillosis |
Drug: Amphotericin B |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Subject) Primary Purpose: Prevention |
Resource links provided by NLM:
Further study details as provided by Capital Medical University:
Primary Outcome Measures:
- invasive pulmonary aspergillosis [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 400 |
| Study Start Date: | June 2008 |
| Estimated Study Completion Date: | October 2010 |
| Estimated Primary Completion Date: | September 2010 (Final data collection date for primary outcome measure) |
Intervention Details:
-
Drug: Amphotericin B
Aerosolized Amphotericin B,2mg/day or 10mg/day
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- 65ys≥age≥18ys
- renal transplant recipients
Exclusion Criteria:
- subjects with hypersensitivity to amphotericin B
- receipt of inhalational or intravenous amphotericin B within last 30 days
- subjects with known invasive fungal infection before renal transplant
- subjects with pneumonia
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00986713
Locations
| China, Beijing | |
| Beijing Chaoyang Hospital,Affiliate of Capital Medical University | Recruiting |
| Beijing, Beijing, China, 100020 | |
| Contact: Bin Cao, doctor 8610-85231130 caobin1999@gmail.com | |
Sponsors and Collaborators
Capital Medical University
More Information
No publications provided
| Responsible Party: | Bin Cao,doctor, Beijing Chaoyang Hospital,Affiliate of Capital Medical Unibersity |
| ClinicalTrials.gov Identifier: | NCT00986713 History of Changes |
| Other Study ID Numbers: | CYH-CMU AmB Neph |
| Study First Received: | September 29, 2009 |
| Last Updated: | September 29, 2009 |
| Health Authority: | China:Beijing Chaoyang Hospital,Affiliate of Capital Medical University |
Additional relevant MeSH terms:
|
Aspergillosis Invasive Pulmonary Aspergillosis Pulmonary Aspergillosis Mycoses Lung Diseases, Fungal Lung Diseases Respiratory Tract Diseases Amphotericin B Liposomal amphotericin B |
Amebicides Antiprotozoal Agents Antiparasitic Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions Antifungal Agents Anti-Bacterial Agents |
ClinicalTrials.gov processed this record on May 23, 2013