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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02622464
Other study ID # 2015-01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 7, 2016
Est. completion date June 7, 2018

Study information

Verified date September 2018
Source Assistance Publique Hopitaux De Marseille
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Post-operative scarring on vocal cords is responsible for disorders of the vibration of the lining to the original dysphonia can be troublesome for the patient both in his private and professional life. There is no currently codified treatment for this type of situation and no therapeutic antifibrotic has been effective. Cell therapy is a promising new approach.After a liposuction and removing of mature adipocytes (40 to 60%), the remaining cells called stromal vascular fraction (SVF) could be isolated. SVF consists of a heterogeneous cell population including multipotent stem cells similar to mesenchymal stem cells present in bone marrow. The investigators hypothesis is that the trophic and antifibrotic properties of SVF could benefit patients with vocal cords scarring responsible for dysphonia.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date June 7, 2018
Est. primary completion date June 7, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Vocal Difficulties felt as crippling (VHI > 60/120)

- Presence of scar hurts of the caused vocal cords is by the initial surgery (micro-laryngoscopy in suspension with or without laser) or by a congenital pathology of glottidis sulcus

- Scar Aspect of vocal cords judged on a stroboscopic examination

- Delay of at least 1 year with regard to the initial surgery

Exclusion Criteria:

- Patients refusing the speech therapy

- Patients operated for a malignant lesion or in malignant potential serious dysplasia of the scar vocal cord

- Contraindication in the anesthesia

- Patients under anti-coagulants

- Patients presenting disorders of the coagulation

- Active infectious diseases

Study Design


Related Conditions & MeSH terms


Intervention

Other:
micro injection of SVF in vocal cords


Locations

Country Name City State
France Assisitance Publique Hopitaux de Marseille Marseille

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary feasibility of Stromal Vascular Fraction injection injected in vocal cords feasibility will be assessed by observation of the immediate volumizing effect on the edge free of the vocal cord appreciated on the video document 13 months
Primary safety will be assessed by the absence of related events related to stromal vascular fraction injection injected in vocal cords safety of Stromal Vascular Fraction injection injected in vocal cords 13 months
Secondary efficiency of SVF injection for the treatment of scarred vocal cords with improved instrumental objective characteristics of the voice of the operated patients efficiency of SVF injection will be assessed by visual analysis of the vocal cord vibration appreciated by vidéolaryngostroboscopy 13 months
Secondary efficiency of SVF injection for the treatment of scarred vocal cords with improved instrumental objective characteristics of the voice of the operated patients efficiency will be assessed by the questionnaire Voice Handicap Index 30 (Jacobson) 13 months
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