Influence of Platelet Concentrates on Wound Healing

NCT ID: NCT03667638

Last Updated: 2018-09-12

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

COMPLETED

Clinical Phase

NA

Total Enrollment

5 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-11-30

Study Completion Date

2017-12-31

Brief Summary

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Chronic soft tissues defects can extend into the fat layer or even deeper and can cause functional disadvantages. Split-thickness skin grafts (STSGs) used to cover these wounds have varying success rates. To improve wound healing in chronic wounds the authors have studied the application of autologous platelet concentrates in a human keratinocyte culture model in vitro and in a combination with surgical procedures in vivo as second line therapy in patients with initially failed wound closure.

Detailed Description

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For in vitro testing on keratinocytes a platelet-mediator concentrate (PMC) was processed with a commercially available bed-side system (ATRĀ®, Curasan, Germany). In a clinical study soft tissue defects (n=5) were treated using a combination of surgical debridement and autologous platelet rich plasma (PRP). Time of healing as determined by epithelization as well as Laser Doppler Imaging to visualize blood flow were analyzed. Additionally, changes in "ease of surgical wound closure" were determined. Finally, the quality of life of patients was assessed using a validated questionnaire.

Conditions

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Platelet-Rich Plasma Wound Healing Delayed

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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PRP Intervention

PRP injection into wound border

Group Type EXPERIMENTAL

Platelet-Rich Plasma

Intervention Type COMBINATION_PRODUCT

Adding PRP to wound bed during surgical debridement

Interventions

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Platelet-Rich Plasma

Adding PRP to wound bed during surgical debridement

Intervention Type COMBINATION_PRODUCT

Other Intervention Names

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PRP, PMC

Eligibility Criteria

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Inclusion Criteria

* exposed tendons, ligaments or bone for \>3 weeks
* no healing tendency

Exclusion Criteria

* sepsis
* intensive care treatment
* continuous smoking
* pregnancy or breast feeding women
* participants of other studies.
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hannover Medical School

OTHER

Sponsor Role lead

Responsible Party

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Paulmann, Anastasia

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Peter Vogt, MD

Role: PRINCIPAL_INVESTIGATOR

Medical School Hannover

Locations

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Medical School Hannover

Hanover, Lower Saxony, Germany

Site Status

Countries

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Germany

References

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Other Identifiers

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#1055-2011

Identifier Type: -

Identifier Source: org_study_id

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