Status:

COMPLETED

PRP Efficacy and Safety in BPF

Lead Sponsor:

Guangzhou Institute of Respiratory Disease

Conditions:

Bronchopleural Fistula

Eligibility:

All Genders

18-75 years

Phase:

NA

Brief Summary

Platelet-rich plasma(PRP), is a concentrate of platelet-rich plasma protein derived from whole blood. The main components of it are platelets, leukocytes and fibrin. Autologous PRP treatment can avoid...

Eligibility Criteria

Inclusion

  • Subjects with aged between 18 to 75
  • Subjects diagnosed with bronchopleural fistula (the sizes of the fistulas less than 4mm)
  • Subjects willing to accept PRP treatment

Exclusion

  • Subjects with fistulas larger than 4mm
  • Subjects who cannot tolerate bronchoscopy due to severe cardiac disease or other major comorbidities
  • Pregnant or breastfeeding women

Key Trial Info

Start Date :

April 16 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

January 25 2024

Estimated Enrollment :

16 Patients enrolled

Trial Details

Trial ID

NCT05304897

Start Date

April 16 2022

End Date

January 25 2024

Last Update

June 21 2024

Active Locations (1)

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Guangzhou Institute of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University

Guangzhou, Guangdong, China, 510120

PRP Efficacy and Safety in BPF | DecenTrialz