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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02174536
Other study ID # DSCHC002
Secondary ID
Status Recruiting
Phase Phase 2
First received June 23, 2014
Last updated June 24, 2014
Start date March 2014
Est. completion date December 2016

Study information

Verified date June 2014
Source Karolinska Institutet
Contact Olle Ringdén, MD, PhD
Phone +46858582672
Email olle.ringden@ki.se
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Interventional

Clinical Trial Summary

A prospective double blind randomized study comparing placenta derived decidual stromal cells with placebo for hemorrhagic cystitis after allogeneic hematopoietic cell transplantation. It is hypothesized that the decidual stromal cell therapy will be superior to placebo.


Description:

Patients with grade 2-4 hemorrhagic cystitis will be randomized to receive either decidual stromal cell therapy at approximately 1x106 cells/kg or placebo on two occasions at weekly intervals. Patients not responsive within 2 weeks will receive decidual stromal cells at approximately 1x106 cells/kg openly.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Hemorrhagic cystitis grade 2-4

- Receives Misoprostol therapy

Exclusion Criteria:

- Patients with urinary urge without macroscopic hematuria or clots

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Intervention

Biological:
Decidual stromal cells
Decidual stromal cells (approximately 1x10^6 cells/kg) will be infused intravenously.
Placebo


Locations

Country Name City State
Sweden Karolinska Institutet Stockholm

Sponsors (1)

Lead Sponsor Collaborator
Karolinska Institutet

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Days to disappearence of macroscopic hematuria or clots Each day, patients fill out a form were they state whether they have macroscopic hematuria or not. 1 month after inclusion No
Secondary Time to disappearance of pain or urges 1 month after inclusion No
Secondary Time to disappearance of microscopic hematuria Each day patients, with the help of a urinary test stick, fill out a form were they state whether they have microscopic hematuria or not. 1 month after inclusion No
Secondary Transplant related mortality All mortality except relapse 1 year after inclusion Yes
Secondary Incidence of severe infections Incidence of severe bacterial, viral or fungal infections. 1 year after inclusion Yes
Secondary Incidence of graft versus host disease One year after inclusion Yes
Secondary Overall actuarial survival Actuarial No
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