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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02195323
Other study ID # Royan-Kidney-004
Secondary ID
Status Completed
Phase Phase 1
First received July 17, 2014
Last updated January 3, 2016
Start date April 2014
Est. completion date January 2016

Study information

Verified date November 2015
Source Royan Institute
Contact n/a
Is FDA regulated No
Health authority Iran: Ethics CommitteeIran: Ministry of Health
Study type Interventional

Clinical Trial Summary

This study was designed to provide confirmation of safety of mesenchymal stem cells (MSCs) therapy in chronic kidney disease (CKD).


Description:

We will assess the 18-month safety and potential efficacy of autologous MSCs as a therapy for CKD. A total of 10 patients with CKD IV injection of high doses 2×106/kg of autologous MSCs t, which will be derived from biopsies of their bone marrow. Assessments will be performed at 1, 3, 6, 12 and 18 months after cell injection. Changes in Glomerular Filtration Rate (GFR) were evaluated by scan isotope.


Recruitment information / eligibility

Status Completed
Enrollment 7
Est. completion date January 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 25 Years to 60 Years
Eligibility Inclusion Criteria:

- Male and Female

- CKD symptoms

- CKD confirmed with serum and urine analysis and GFR 25-60 mL/min/1.73 m2

- Patient's age between 25 - 60 years

- Ability to understand and willingness to sign consent from

Exclusion Criteria:

- Pregnant or lactating

- Basis disease such as diabetes, malignancy and autoimmune

- Unable to follow post-operative exercise regimen or return for evaluations

Study Design

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


Intervention

Biological:
Intravenous injection
Intravenous injection of bone marrow derived MSC in patients with CKD.

Locations

Country Name City State
Iran, Islamic Republic of Royan Institute Tehran

Sponsors (1)

Lead Sponsor Collaborator
Royan Institute

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary mass formation Evaluation the probability of mass formation due to MSC transplantation 6 months after cell injection. 6months Yes
Primary Creatinin Evaluation the rise of creatinin 1 month after cell transplantation. 1 month Yes
Secondary GFR Evaluation the increase of GFR 6 months after cell transplantation with scan isotope . 6months Yes
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