- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02961725
Stem Cells for Treatment of Bronchopleural Fistula
Umbilical Cord Mesenchymal Stem Cells for Treatment of Bronchopleural Fistula
Bronchopleural fistula (BF), an abnormal passage or communication between a bronchus and another part of the body, may develop when there are penetrating wounds of the thorax and after lung surgery. Without effective therapy, treatment of BF is a challenge, with a high rate of mortality and teratogenicity.
The investigators will conduct endoscopic injection of umbilical cord mesenchymal stem cells to fistula, observe the recovery of bronchopleural fistula and systemic reactions, to investigate the application of umbilical cord mesenchymal stem cells in the treatment of bronchopleural fistula.
Study Overview
Study Type
Enrollment (Anticipated)
Phase
- Phase 1
Contacts and Locations
Study Contact
- Name: Yimin Zeng, Dr.
- Phone Number: 0595-22766122
- Email: zeng_yi_ming@126.com
Study Locations
-
-
Fujian
-
Quanzhou, Fujian, China, 362000
- Recruiting
- The Second Affiliated Hospital of Fujian Medical University
-
Contact:
- Hongzhi Gao, Dr.
- Phone Number: 0595-22766122
- Email: 1564747628@qq.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- diagnosed with bronchopleural fistula by imaging or bronchoscopic examination
- typical symptom of bronchopleural fistula, such as fever, cough, purulent sputum, weight loss…
- patients present compromised conditions, who can only accept a conservative treatment.
Exclusion Criteria:
- absolute contraindication of bronchoscopic examination and treatment
- with previous treatment of cell therapy, including stem cells.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: UCMSC treatment
UCMSC: umbilical cord mesenchymal stem cells
|
UCMSC: umbilical cord mesenchymal stem cells 3-5*10^7/5 ml
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
closure of the fistula
Time Frame: 24 weeks
|
median time for fistula closure
|
24 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
complication
Time Frame: 1 year
|
fever, coughing up blood, infection...
|
1 year
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Yimin Zeng, Dr., The Second Affiliated Hospital of Fujian Medical University
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SC-BF
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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Marie Hudson, MDAssistance Publique - Hôpitaux de Paris; Medical University of South Carolina; Centre hospitalier de l'Université de Montréal (CHUM) and other collaboratorsRecruitingMesenchymal Stem Cells | Sclerosis, SystemicCanada