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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02325843
Other study ID # 2014MEKY059
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date July 2015
Est. completion date December 2017

Study information

Verified date April 2019
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Ocular chemical burn is one of the cause of vision loss in our country, and there are no satisfactory treatment. Human bone marrow mesenchymal stem cells (MSC) have the biological characteristics of self-renewal, immune regulation, multidirectional differentiation and tissue repair. Our preliminary research showed that in corneal alkali injury rats, the MSC can accelerated the cornea repair, inhibited angiogenesis. The aim of this study is to access the efficacy and safety of mesenchymal stem cell in the treatment of corneal burn in human.


Description:

Corneal burn is a ocular damage disease included chemically burned and thermally burned. Surgery of corneal transplantation,amniotic membrane transplantation are some of effective,however,these therapy are expensive and the transplantation resources are limited. To arrest the inflammatory phase, several types of immunosuppressive treatments have been investigated. Corticosteroids also is important, however, long time usage of corticosteroids often cause severe side-effects. Human bone marrow mesenchymal stem cells (MSC) have the biological characteristics of self -renewal, immune regulation, multidirectional differentiation and tissue repair. Our preliminary research showed that in corneal alkali injury rats, the MSC can accelerated the cornea repair, inhibited angiogenesis. Many animal research also revealed that MSC have effect on the ocular alkali burned. And subconjunctivity injection is efficient, the clinical study of MSC on treating other disease have been developed rapidly recently, in further ,the outcome are encouraging, and no side-effect related MSC was reported, MSC can come from bone marrow, Umbilical cord blood,Adipose tissue and so on, but bone marrow MSC is mostly common used. The investigators propose to assess the efficacy and safety of human bone marrow mesenchymal stem cell in the treatment of corneal burn in human.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

1. must be ocular burns including chemically burned or the thermally burned

2. the severity degree should above the ? degree,including the ? degree(according the classification of Dua standard,2001)

3. the subjects are willing to accept this research,and promise to coordinate with the researchers during the follow up period

4. the subjects should abide by the laws and rules of the study.

5. the incident time should be within 2 weeks -

Exclusion Criteria:

1. the visual acuity is blind in any of the eye

2. have corneal perforation or have the corneal perforation tendency

3. have been accepted surgury on eyeball after trauma

4. IOP=25mmHg even after antiglaucoma

5. have the history of other corneal diseaze or surgury

6. have the history of radiotherapy or surgury in the eyeball

7. associated with corneal ulcer or endoophthalmitis

8. uncontrolled hypertension(=150/95mmHg)

9. abnormal liver and renal function

10. the pregancy women -

Study Design


Related Conditions & MeSH terms


Intervention

Other:
human bone marrow MSC
The arms of active comparator :human bone marrow MSC subconjunctival injection once time. If persistent epithelial defect was noted thereafter, a second MSC injection was performed.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-sen University

References & Publications (3)

Gao XH, Roberts A. The left triangular ligament of the liver and the structures in its free edge (appendix fibrosa hepatis) in Chinese and Canadian cadavers. Am Surg. 1986 May;52(5):246-52. — View Citation

Hargraves MM. Discovery of the LE cell and its morphology. Mayo Clin Proc. 1969 Sep;44(9):579-99. — View Citation

Le Blanc K, Mougiakakos D. Multipotent mesenchymal stromal cells and the innate immune system. Nat Rev Immunol. 2012 Apr 25;12(5):383-96. doi: 10.1038/nri3209. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of adverse events by subconjunctival injection of BMMSCs Record the adverse events, including topical complications such as ocular infection, conjunctival necrosis at the injection site, retinal artery occlusion, and systemic complications such as fever, urticaria, hemolysis, hypotension, renal and liver dysfunction, tumor formation, and/or abnormalities in complete blood counts. 6 months
Secondary Incidence of corneal perforation rate after subconjunctival injection of BMMSCs the number of corneal perforation eyes/total eyes 6 months
Secondary Time of corneal epithelialization record the time when cornea finish epithelialization 6 month
Secondary Visual acuity Use the visual chart to record the decimal visual acuity 6 month
See also
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