SVF Combined With Functional Self-assembling Peptide Nanofiber Hydrogels in the Treatment of Spinal Cord Injury

NCT ID: NCT05967325

Last Updated: 2023-08-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-07-15

Study Completion Date

2025-07-15

Brief Summary

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Traumatic spinal cord injury (SCI) is a severe medical problem experienced by people worldwide with high mortality and long term morbidity. Although progress has been made in understanding cellular and molecular mechanisms of SCI, treatment and management protocols aimed at ameliorating neurologic damage in patients remain ineffective. Cells and biomaterials offer new hope for the treatment of SCI.

Up to now, there have been many studies on the treatment of SCI using cells and biomaterials. Stromal Vascular Fraction (SVF) is a heterogeneous mixture of cells obtained from adipose tissue. These cells include adipose-derived stem cells, endothelial cells, endothelial progenitor cells, pericytes, T cells, and other immune cells. SVF has strong self-renewal, proliferation and differentiation potential, it can replace necrotic cells and synthesize a variety of bioactive factors through paracrine and autocrine, activate cell and vascular regeneration pathways. Therefore, SVF shows significant advantages. The sequence of functional self-assembling peptide nanofiber hydrogels (hereinafter referred to as hydrogels) is HGF(RADA)4RIKVAV (H: histidine; G: Glycine; F: phenylalanine; R: arginine; A: Alanine; D: aspartic acid; I: isoleucine; K: Lysine; V: valerine). The hydrogel is based on the short peptide RADA16 ((RADA)4, which is already available in the product PuramatrixTM for clinical hemostasis and cell culture, but the aqueous solution of PuramatrixTM is acidic which harms cells and tissues upon direct contact. While the hydrogels in this study is pH neutral and does not harm cells and tissues. Articles published by the provider demonstrate that hydrogels can support 3D stem cell growth, have good biocompatibility in vivo (animal spinal cord), and promote neural regeneration after SCI. The chemical structure of the hydrogels is simple and clear, and the degradation product is amino acid. Therefore, SVF and the hydrogel from functional self-assembling peptide are combined for SCI repair in the study.

Detailed Description

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Conditions

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Safety Issues

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Stromal Vascular Fraction (SVF) combined with Functional self-assembling peptide nanofiber hydrogels

Transplantation of SVF and biomimetic nanohydrogel

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. Male or female adults, 18-60 years of age, with a clinical diagnosis of chronic traumatic SCI (≥ 3 months after SCI)
2. Neurological examination: ASIA-A
3. Both the spinal and neurological levels of injury were between T1-T12
4. Subjects must be able to read, write and complete visual analogue scale
5. Voluntarily signs and dates an informed Consent form, approved by an Institutional Review Board (IRB)/Independent Ethics Committee (IEC), prior to any study-specific procedures.

Exclusion Criteria

1. Subjects with osteoporosis or had joint disease
2. Severe head injury
3. Severe pressure sore
4. Sign of kidney, cardiovascular, liver disorders
5. Subjects with internal medical and/or infectious diseases (including but not limited to Hepatitis B and HIV carriers)
6. Pregnant women or women at lactation stages
7. Medically or mentally unstable according to the judgment of the investigator
8. History of multiple sclerosis or peripheral demyelination
9. Any criteria which, in the opinion of the investigator, suggests that the subject would not be compliant with the study protocol
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kunming Tongren Hospital

INDUSTRY

Sponsor Role lead

Responsible Party

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Hui Zhu

Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Kunming Tongren Hospital

Kunming, Yunnan, China

Site Status RECRUITING

Countries

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China

Central Contacts

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HUI ZHU

Role: CONTACT

(86)13888092115

Facility Contacts

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Hui Zhu, MD

Role: primary

(86)13888092115

Other Identifiers

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KunmingTH_HZ_003

Identifier Type: -

Identifier Source: org_study_id

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