MicroCutter Assisted Thoracic Surgery Hemostasis Registry

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02816671

Acronym

MATCH

Enrollment

100

Registered

2016-06-28

Start date

2016-06-30

Completion date

2018-09-30

Last updated

2018-09-10

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

Conditions

Lobectomy, Segmentectomy

Brief summary

The primary purpose of this prospective, open-label, multi-center observational registry with all-comers enrollment is to report on the use of the MicroCutter Stapler in a real world setting in thoracic surgical procedures. Procedures may be open or video assisted thoracic surgery (VATS) including robotic surgical cases. Clinicians will provide objective and subjective evaluation of the use of the stapler in their procedures.

Detailed description

The MATCH registry is a prospective, open label, multi-center observational registry with enrollment of patients requiring surgical stapling during a lobectomy or segmentectomy. Patients will be treated per the clinicians standard of care with medical history and demographic data collected pre-procedure, operative data including clinician's objective and subjective evaluation of the stapler and confirmation of any complications via query and data collection at hospital discharge and each clinician's standard post-operative contact.

Interventions

DEVICESurgical Stapler

Patients in whom the MicroCutter stapler was used during a thoracic surgical procedure.

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

* Patients undergoing lobectomy/segmentectomy in which the MicroCutter Stapler and Reloads were used. * Patient is willing and able to sign informed consent form to participate in registry, allowing for collection of data.

Exclusion criteria

* Clinician determines no vessels are suitable for the on label use of the MicroCutter Stapler and Reloads.

Design outcomes

Primary

Measure	Time frame	Description
Hemostasis of vessel staple line	through study completion, approximately 1 month	Objective classification of hemostasis achieved by the MicroCutter Stapler used on label using a Likert like scale; from 1 (no bleeding) to 5 (bleeding requiring conversion to open procedure or discovered post operatively)

Countries

United Kingdom

Outcome results

None listed

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