Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02304562
Other study ID # CHIN-PLAGH-ST-004
Secondary ID
Status Recruiting
Phase Phase 1
First received November 21, 2014
Last updated December 1, 2014
Start date January 2013
Est. completion date December 2017

Study information

Verified date November 2014
Source Chinese PLA General Hospital
Contact xiaobing FU
Phone +86(10)937516
Is FDA regulated No
Health authority China: Ethics Committee
Study type Interventional

Clinical Trial Summary

Patients with skin injury treated with Umbilical Cord Blood-derived Mesenchymal Stem Cells,such as deep burn damaged sweat glands,Effectiveness of Umbilical Cord Blood-derived Mesenchymal Stem Cells in Regeneration of Sweat Glands and Body Repair is determined.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Burn area:10-20%TBSA

Exclusion Criteria:

- Have influence on the speed of wound healing of patients with chronic diseases

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Biological:
UCB Mesenchymal Stem Cells treatment
reduce skin injury

Locations

Country Name City State
China Chinese PLA General Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Chinese PLA General Hospital

Country where clinical trial is conducted

China, 

References & Publications (1)

Fu X, Qu Z, Sheng Z. Potentiality of mesenchymal stem cells in regeneration of sweat glands. J Surg Res. 2006 Dec;136(2):204-8. Epub 2006 Oct 20. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Frequency of Adverse Events Frequency and severity of Adverse Events 6 months Yes
Secondary Active and inactive lesion count 6 months Yes
See also
  Status Clinical Trial Phase
Recruiting NCT05102396 - Topical Oxybutynin for Treatment of Hyperidrosis: Local or Systemic Effect? Phase 2
Completed NCT04906655 - An Open Label Study for Palmar Hyperhydrosis Phase 2
Recruiting NCT03426085 - The Effects of Liraglutide on Sudomotor Function and Inflammation in Type 2 Diabetes Phase 2
Enrolling by invitation NCT01539460 - A Minimally Invasive Surgery for Axillary Osmidrosis: Combined Liposuction With Subcutaneous Pruning N/A