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Pilot Study of Stem Cell Treatment of Patients With Vocal Fold Scarring

Primary Purpose

Improved Healing of Scarred Vocal Folds, Improved Vocal Fold Status, Improved Vocal Fold Function

Status
Completed
Phase
Phase 1
Locations
Sweden
Study Type
Interventional
Intervention
aMSC
aMSC+hyaluronan gel
Sponsored by
Karolinska University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Improved Healing of Scarred Vocal Folds focused on measuring vocal fold scarring, mesenchymal stem cells

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • severe hoarseness
  • vocal fold scarring
  • no active other treatment
  • age above 18 years

Exclusion Criteria:

  • active treatment of laryngeal disorder
  • active inflammatory condition of the larynx
  • diagnosed or suspicions of local malignancy

Sites / Locations

  • Karolinska University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

aMSC with and without hyaluronan gel

Arm Description

autologous mesenchymal stem cells (aMSC) injected into the vocal folds in 8 patients and aMSC mixed with hyaluronan gel in 8 patients

Outcomes

Primary Outcome Measures

Improved healing of scarred vocal folds
Laryngeal and general ear, nose, and throat status will be followed for each patient at least one year after primary treatment. This includes examination of signs of local (laryngeal) inflammatory reaction/defect healing, e.g. polyp or granuloma formation, inflammatory reaction after local aMSC injection It also includes repetitive examinations of vocal fold function and voice function including high speed examination of the vocal folds, acoustic voice analysis and phonation pressure measurements as well as subjective ratings by means of Voice handicap index scale

Secondary Outcome Measures

Full Information

First Posted
November 5, 2013
Last Updated
February 24, 2020
Sponsor
Karolinska University Hospital
Collaborators
The Swedish Research Council, Laryngfonden, Karolinska Institutet
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1. Study Identification

Unique Protocol Identification Number
NCT01981330
Brief Title
Pilot Study of Stem Cell Treatment of Patients With Vocal Fold Scarring
Official Title
Pilot Study of Patients With Severe Hoarseness and Vocal Fold Scarring Treated With Mesenchymal Stem Cells With and Without Hyaluronan Gel
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
February 24, 2020 (Actual)
Study Completion Date
February 24, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska University Hospital
Collaborators
The Swedish Research Council, Laryngfonden, Karolinska Institutet

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a pilot-study of 16 selected Swedish patients which all have severe hoarseness or aphonia due to vocal fold scarring (from previous surgery, radiation therapy, inflammation or possibly hereditary). The patients are operated with phonomicrosurgical dissection of the scarred vocal folds, removal or scar tissue and injection of autologous mesenchymal stroma cells, aMSC (which were previously harvested from each patients´s bone marrow, purified, expanded and characterized according to standard procedure at the Center of Hematology and Regenerative Medicine Karolinska University Hospital Huddinge). 8 Patients is planned to be treated with a single injection of aMSC and 8 patients with injection of aMSC mixed with a carrier hyaluronan gel developed at Uppsala University Sweden and at the Karolinska Institute. The laryngeal status, vocal fold function, and voice function will be followed individually with an advanced battery of examinations performed before and up to 1 year postoperatively. Side effects and complications are noted and reported during surgery and following surgery at regular intervals during at least 1 year Since spring 2015 no new patients have been recruited and no treatments are given during 2016 or 2017. The monitoring authority was changed from Swedish National Board of Health to Swedish Medical Product Agency (MPA) in March/April 2016. Further inclusions and treatments are postponed until permission is granted from MPA to continue the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Improved Healing of Scarred Vocal Folds, Improved Vocal Fold Status, Improved Vocal Fold Function
Keywords
vocal fold scarring, mesenchymal stem cells

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
aMSC with and without hyaluronan gel
Arm Type
Experimental
Arm Description
autologous mesenchymal stem cells (aMSC) injected into the vocal folds in 8 patients and aMSC mixed with hyaluronan gel in 8 patients
Intervention Type
Biological
Intervention Name(s)
aMSC
Intervention Description
aMSC injected into the vocal fold of the patient
Intervention Type
Biological
Intervention Name(s)
aMSC+hyaluronan gel
Intervention Description
aMSC+ hyaluronan gel is injected into the patients vocal fold
Primary Outcome Measure Information:
Title
Improved healing of scarred vocal folds
Description
Laryngeal and general ear, nose, and throat status will be followed for each patient at least one year after primary treatment. This includes examination of signs of local (laryngeal) inflammatory reaction/defect healing, e.g. polyp or granuloma formation, inflammatory reaction after local aMSC injection It also includes repetitive examinations of vocal fold function and voice function including high speed examination of the vocal folds, acoustic voice analysis and phonation pressure measurements as well as subjective ratings by means of Voice handicap index scale
Time Frame
1 year postoperatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: severe hoarseness vocal fold scarring no active other treatment age above 18 years Exclusion Criteria: active treatment of laryngeal disorder active inflammatory condition of the larynx diagnosed or suspicions of local malignancy
Facility Information:
Facility Name
Karolinska University Hospital
City
Stockholm
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
32197630
Citation
Hertegard S, Nagubothu SR, Malmstrom E, LeBlanc K. Treatment of vocal fold scarring with autologous bone marrow-derived human mesenchymal stromal cells-first phase I/II human clinical study. Stem Cell Res Ther. 2020 Mar 20;11(1):128. doi: 10.1186/s13287-020-01632-8.
Results Reference
derived

Learn more about this trial

Pilot Study of Stem Cell Treatment of Patients With Vocal Fold Scarring

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