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OpenTrials
Completed

NCT Number: NCT03526913

Role of Platelet Rich Plasma in Enhancing Graft Take in Chronic Venous Ulcers

Chronic venous ulcers are considered a problem with a big morbidity impact on both the health facilities and patients, skin-grafting have shown not so perfect outcomes with such ulcers. In this study, the investigators compare combining autologous platelet rich plasma treatments with partial skin grafting in chronic ulcers, the results were compared to using only partial skin grafting, and among various types of chronic resistant ulcers.

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Key information

Age range

12 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

About this study

Fourteen patients had bilateral lower limb ulcers, and 6 of them had single large ulcers as follows; Fourteen patients with chronic venous ulcers (12 of which had bilateral ulcers, 2 had single large ulcers) Four patients, each with a single chronic post-traumatic ulcer Two patients with bilateral chronic lymphatic ulcers.

After detailed history, physical examination and investigations (such as duplex),

  • Each patient with bilateral ulcers included in the study (14 patients) received treatment A on one ulcer and treatment B on the other ulcer.
  • In case of patients with single large ulcers (6 patients), treatment A was done on one half of the ulcer and treatment B on the other half of the ulcer (done in ulcers with an area greater than 10 x 10 cms).
  • Treatment A included pre-operative intra-lesional PRP injections in 1-week intervals for 3 times, followed by intra-operative intra-lesional injection of PRP prior to meshed graft placement. PRP was injected into the ulcer bed and ulcer edges using a sterile syringe.

Treatment B included only placement of meshed graft, with no PRP treatment.

  • Pre-operative preparation: Ulcers were prepared by proper dressings and followed up until acquiring a clean bed. Debridement was done as needed to obtain clean base ready for graft placement.
  • PRP preparation:
  • 10 ml of blood was drawn from each patient intra operatively (autologous PRP).
  • Blood was collected in sterile tubes, Anticoagulant Citrate Dextrose (ACD) was used for anticoagulation, which is the same substance used to preserve viable platelets in blood banks for platelet transfer.
  • Tubes were centrifuged in Beckman Allerga X-12 centrifuge for 20 mins, 3000 rpm.
  • Each 10 ml of blood yielded an average of 3-4 ml of PRP. Calcium gluconate was added in a ratio of 1:10 to PRP. Post-operative assessment was carried out by follow up clinical examination, photography and weekly biopsy samples.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with chronic ulcers for at least 6 months.
  • Age ≧ 12 years.

Exclusion criteria

  • Patients younger than 12 years of age.
  • Patients with diabetes or other diseases affecting tissue healing.
  • Patients with current ongoing pathologies in arterial or venous systems.
  • Patients with malignant ulcers.
  • Patients on corticosteroids or other drugs affecting tissue healing.
  • Patients with unrealistic expectations.

Treatment and study plan

PRP

Procedure

PRP: autologous platelet-rich plasma

Other names: platelet rich plasma

STSG

Procedure

skin graft: Split Thickness Skin Grafting (STSG)

Other names: split thickness skin graft

Primary outcomes

  1. Graft take

    Time frame: month

    percentage of graft take

Sponsors and collaborators

Lead sponsor

Noha Mohsen Omar

Other

Collaborators

  • Menoufia University

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2018
First posted
May 16, 2018
Registry last updated
May 18, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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