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Platelet-Rich and Concentrated Platelet-Poor Plasma to Reduce Air Leak Post-Lobectomy: A Randomized Controlled Trial

Platelet-Rich and Concentrated Platelet Poor Plasma to Reduce Air Leak Post Lobectomy: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00665912
Enrollment
204
Registered
2008-04-24
Start date
2008-01-31
Completion date
2010-11-30
Last updated
2017-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Brief summary

The purpose of this study is to determine whether the use of platelet-rich plasma (PRP) and concentrated platelet-poor plasma (PPPc) can reduce the duration of post-operative air leak after lobectomy for lung tumours.

Interventions

PROCEDUREStandard post-lobectomy wound care plus use of PRP and PPPc prepared by GPS and Plasmax respectively

GPS is used to create the platelet rich plasma (PRP). Plasmax is used to create the concentrated platelet-poor plasma (PPPc). Both PRP and PPPc will be used for wound care in the thoracic cavity post-lobectomy.

PROCEDUREStandard post-lobectomy wound care

Standard post-lobectomy wound care

Sponsors

University of Western Ontario, Canada
CollaboratorOTHER
Zimmer Biomet
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients requiring a lobectomy

Exclusion criteria

* Pneumonectomy * Sleeve lobectomy * Determination of unresectability (prior to the initiation of lobectomy) * Wedge resection alone

Design outcomes

Primary

MeasureTime frame
Duration of postoperative air leakEvery 4 hours of postop hospital stay, between 4-6 weeks postop

Secondary

MeasureTime frame
Incidence of air leak, Prolonged air leak (> days), ComplicationsEvery 4 hours of postop hospital stay, between 4-6 weeks postop

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026