DRKS00022202
Completed
N/A
Protective Variable Controlled Ventilation during One Lung Anesthesia (PROVALUNG) – A Randomized Controlled Trial - PROVALUNG
ConditionsIntraoperative one-lung ventilation
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Intraoperative one-lung ventilation
- Sponsor
- Technische Universität Dresden
- Enrollment
- 78
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients with planned thoracic surgery (open or video\-assisted) under one\-lung ventilation using a double lumen tube and invasive monitoring of arterial blood pressure
- •\- ASA \= 3
- •\- Planned duration of intervention \> 30 min
- •\- Age \= 18
- •\- Weight \> 40 kg
- •\- Written consent of the participating person
Exclusion Criteria
- •\- COPD GOLD grade 3 and 4
- •\- Untreated asthma
- •\- Lung separation using a method other than DLT (e.g. difficult airway, tracheostomy)
- •\- Contraindications against total intravenous anaesthesia
- •\- History of hypersensitivity/allergy to one of the medications to be used or their ingredients or to medication with a similar chemical structure
- •\- Participation of the patient in another clinical trial within the last 4 weeks before inclusion
- •\- Addictions or other illnesses which do not allow the person concerned to assess the nature and extent of the clinical trial and its possible consequences
- •\- Pregnant or breastfeeding women
- •\- Women of childbearing age, except women who meet the following criteria:
- •\> Post\-menopausal (12 months natural amenorrhoea or 6 months amenorrhoea with serum FSH \> 40 mlU/ml)
Outcomes
Primary Outcomes
Not specified
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