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Adipose Mesenchymal Stem Cells (AMSC) for Treatment of Ulcerative Colitis

A Phase I/II Randomized, Controlled, Clinical Trial for Assessment of the Safety and Efficacy of Allogeneic Adipose Mesenchymal Stem Cells in Moderate to Severe Ulcerative Colitis Patients

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03609905
Acronym
AMSC_UC
Enrollment
50
Registered
2018-08-01
Start date
2018-07-01
Completion date
2021-12-01
Last updated
2020-09-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ulcerative Colitis (UC)

Keywords

ulcerative colitis (UC), mesenchymal stem cells(MSC)

Brief summary

Ulcerative colitis is a form of inflammatory bowel disease characterized by diffuse inflammation of the colonic mucosa. It affects the rectum and extends proximally along a variable length of the colon. Ulcerative colitis is a chronic condition with a relapsing remitting course. Mesenchymal stem cells (MSCs) are a subset of adult stem cells residing in many tissues, including bone marrow (BM), adipose tissue, umbilical cord blood. Recent experimental findings have shown the ability of MSCs to home to damaged tissues and to produce paracrine factors with anti-inflammatory properties, potentially resulting in reduction of inflammation and functional recovery of the damaged tissues. The purpose of our study is to evaluate safety and efficacy of the intracolonic injection by using a colonoscope of allogeneic adipose MSCs in patients with moderate active ulcerative colitis.

Interventions

BIOLOGICALAdipose-cord mesenchymal stromal cells (A-MSCs)

A-MSCs 5 x 10\ 7 diluted on 100 mL of normal saline

5-amino-salicylic acid or glucocorticoid

Sponsors

Liaocheng People's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Male or female, 18-65 years old * Diagnosis of ulcerative colitis diagnosed at least 6 months earlier * Moderate or severe activity defined by a Mayo score * No serious infection, chronic diseases, diabetes and tuberculosis * Unefficient by using 5-ASA, glucocorticoid or azathioprine * Written informed consents were obtained from all subjects * Capable of good communication with researchers and follow the entire test requirements * Negative pregnancy test for women of childbearing potential (from menarche to menopause)

Exclusion criteria

* Pregnant or breastfeeding women or cognitively impaired adults * History of malignant disease * Infectious colitis * Patients with known allergies to culture medium * Patients having participated in clinical trials with any investigational drug within 1 month prior to enrolment in this study * Patients with suspicion of Crohn's enterocolitis, indeterminate colitis, ischaemic colitis, radiation colitis, diverticular disease associated colitis, or microscopic colitis * Patients with previous colectomy * Positive to one or more of the infectious disease panel * Treatment with surgery or biological treatment (infliximab or adamizumab) or Cyclosporine or tacrolimus or mycophenolate in the 8 weeks prior to inclusion in the study * Presence of severe concomitant diseases * Patients with clostridium difficult or cytomegalovirus infection

Design outcomes

Primary

MeasureTime frameDescription
Change From Baseline in Endoscopic Score (as Measured by Ulcerative Colitis Endoscopic Index of Severity)Baseline, 8 weeksUlcerative Colitis Endoscopic Index of Severity (UCEIS) is defined as Ulcerative Colitis Endoscopic Index of Severity, with higher scores indicating more severe disease

Secondary

MeasureTime frameDescription
Change from Baseline in clinical response (CDAI points)Baseline, 8 weeksCDAI is defined as Clinical Disease Activity Index
To evaluate the quality of life index, Short Inflammatory Bowel Disease Questionnaire (SIBDQ)Baseline, 8 weeksThe Short Inflammatory Bowel Disease Questionnaire (SIBDQ) is a health-related quality of life (HRQoL) tool measuring physical, social, and emotional status. It includes 10-item form of questions. Each question is scored on a Likert scale from 1 (worst) to 7 (best), scores from each item are summed to produce a total score, increased more than 3 scores were considered remission.
Histologic Evaluation of Ulcerative ColitisBaseline, 8 weeksA 10 to 20 centimeter (cm) biopsy sample of inflamed mucosal tissue was taken from the worst affected area and scored using the Riley Index. The Riley Index is a histologic scoring system for the assessment of the activity and severity of ulcerative colitis, ranging from 0 to 24. It consists of 6 histologic features (acute inflammatory cell infiltrate, crypt abscesses, mucin depletion, surface epithelial integrity, chronic inflammatory cell infiltrate, and crypt architectural irregularities), all scored on a 4-point scale (higher scores indicate more severe disease).
Immune response in ulcerative colitis.Baseline, 1, 4, 8 weeksA number of soluble mediators are detected, including proinflammatory cytokines (TNF, IFN-γ, IL-6.) and anti-inflammatory cytokines (IL-10, IL-4.).
Incidence of Treatment Adverse.Baseline, 1, 4, 8 weeksAn AE was any untoward medical occurrence in a participant

Countries

China

Contacts

Primary ContactShaoda Ren, Ph.D.
zslrsd@163.com86-0635-8272202

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026