Hemothorax; Traumatic Clinical Trial
Official title:
Video_ Assisted Thoracoscopic Surgery Evacuation Compared to Reinsertion of Thoracostomy Tube in Persistent Traumatic Haemothorax
This is prospective, randomized study comparing VATS (video- Assisted Thoracoscopy) to reinsertion of a thoracostomy tube in patients with persistent traumatic haemothorax. The incidence varies and can be as high as 20%, but in most studies is found to be 1-4% after initial tube thoracostomy for chest trauma. The most accepted complication of retained hemothorax is empyema.Retained hemothorax treatment started by physiotherapy and early withdrawal of tube thoracostomy which lead to more complications as empyema, fibro thorax/entrapped lung, flail chest and diaphragmatic hernia. Early VATS is an alternative treatment for retained hemothorax with evidence that it is a superior intervention when compared to a second tube thoracostomy.
Status | Recruiting |
Enrollment | 2 |
Est. completion date | July 30, 2018 |
Est. primary completion date | July 30, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: We include for the study all patients admitted to Assiut university hospitals during the time of the study that proved persistent haemothorax that with criteria: 1. Ages that are eligible for study are between 18years to 60 years (adult) 2. Both genders will be included to study. 3. Clinical and radiological diagnosis of persistent haemothorax. 4. Thoracostomy tube blockage or failure to drain within 5-7days. Exclusion Criteria: 1. More than one thoracostomy tube drainage in the same attempt side. 2. Unable to consent to trial. 3. Coexisting pathology requiring other interventions. 4. Patients that need urgent interventions (hemodynamically unstable, empyema and flail chest). |
Country | Name | City | State |
---|---|---|---|
Egypt | Assiut university | Assiut |
Lead Sponsor | Collaborator |
---|---|
Assiut University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Duration of hospitalization | number of days spent | average 5-7 days | |
Secondary | number of patients developed empyema | the study will be monitored for septic complications , specially empyema. | through one month |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04006587 -
IS Reduces Rib Fracture Complications
|
N/A | |
Not yet recruiting |
NCT04098185 -
Role of Pleural Fluid Attenuation Value on CT as a Diagnostic Tool in Traumatic Hemothorax
|