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VATS ( Video-Assisted Thoracoscopy) Compared to Reinsertion of a Thoracostomy Tube for Persistent Haemothorax

VATS( Video-Assisted Thoracoscopy ) Compared to Reinsertion of a Thoracostomy Tube for Persistent Haemothorax A Single Center Prospective Randomized Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02014077
Enrollment
62
Registered
2013-12-17
Start date
2014-01-31
Completion date
2019-11-30
Last updated
2020-01-29

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

Conditions

Empyema, Haemothorax

Keywords

VATS( Video-Assisted Thoracoscopy ), Thoracostomy Tube, Empyema, Thoracotomy

Brief summary

This is a prospective, randomized study comparing VATS( Video-Assisted Thoracoscopy ) to reinsertion of a Thoracostomy Tube in patients with retained haemothorax. The hypothesis is that early VATS as opposed to reinsertion of a thoracostomy tube , will lead to less complications and shorter hospital stay.

Interventions

PROCEDUREVATS ( Video-Assisted Thoracoscopy )

the patients were randomized to a Video-Assisted thoracoscopy( VATS )for retained haemothorax

PROCEDUREThoracostomy Tube reinsertion

the patient is randomized to reinsertion of a Thoracostomy Tube for retained haemothorax

Sponsors

University of Cape Town
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Clinical and radiological diagnosis of retained haemothorax * Thoracostomy tube blockage or failure to drain

Exclusion criteria

* more than one attempt at thoracostomy tube drainage * unable to consent to trial * coexisting pathology requiring other interventions

Design outcomes

Primary

MeasureTime frameDescription
duration of hospitalizationpatients will be followed during their hospital stay, average 5-14 daysnumber of days spent in hospital

Secondary

MeasureTime frameDescription
number of patients that develop empyema2 months form initial injuryeach arm of the study will be monitored for septic complications , specifically empyema of the pleural cavity

Other

MeasureTime frameDescription
number of patients requiring thoracotomy2 months from initial injurythe patients that develop empyema will require a thoracotomy for clearance of the pleural cavity

Countries

South Africa

Outcome results

None listed

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