Peak airway pressure (Ppeak-mmHg) will be recorded before initiation of OLV and 30 minutes intervals up to 120 minutes after initiation of OLV. Change from initiation of Ppeak at 120 minute will be evaluated.
Effect Of Ketamine Infusion In Patients With COPD Applied One Lung Ventilation
Brief Summary
Intervention / Treatment
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Ketamine (DRUG)After induction, patients will be received 1 mg/kg ketamine bolus, then administered 0,5 mg/kg/hour ketamine infusion intraoperatively.
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Saline (DRUG)After induction, patients will be received saline bolus, then will be administered saline infusion intraoperatively.
Condition or Disease
- Chronic Obstructive Pulmonary Disease Mild
- Chronic Obstructive Pulmonary Disease Moderate
- Chronic Obstructive Pulmonary Disease Severe
- Lungcancer
- Anesthesia
Phase
Study Design
Study type: | INTERVENTIONAL |
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Status: | Completed |
Study results: | No Results Available |
Age: | 40 Years to 80 Years |
Enrollment: | 30 (ACTUAL) |
Funded by: | Other |
Allocation: | Randomized |
Primary Purpose: | Prevention |
MaskingDOUBLE:
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Clinical Trial Dates
Start date: | Jan 01, 2017 | ACTUAL |
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Primary Completion: | Mar 01, 2018 | ACTUAL |
Completion Date: | Mar 01, 2018 | ACTUAL |
Study First Posted: | Nov 15, 2016 | ESTIMATED |
Results First Posted: | Aug 31, 2020 | |
Last Updated: | May 26, 2018 |
Sponsors / Collaborators
Location
Participant Groups
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After induction, patients will be received 1 mg/kg ketamine bolus, then will be administered 0,5 mg/kg/hour ketamine infusion intraoperatively. Anesthesia will be maintained with %4-6 desflurane and 0,25-0,5 microgram/dk/min remifentanil.
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After induction, patients will be received saline bolus, then will be administered saline infusion intraoperatively. Anesthesia will be maintained with %4-6 desflurane and 0,25-0,5 microgram/dk/min remifentanil.
Eligibility Criteria
Sex: | All |
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Minimum Age: | 40 |
Maximum Age: | 80 |
Age Groups: | Adult / Older Adult |
Healthy Volunteers: | Yes |
* Age more than 40 years
* American Society of Anesthesiologists' physical status 2-3
* Diagnosis of COPD
* Forced expiratory volume in 1 second (FEV1) ≥ %50 in a preoperative pulmonary function test.
Exclusion Criteria:
* Heart failure
* Severe functional liver or kidney disease
* Pregnancy,
* Obesity (BMI≥30)
* Respiratory failure (Pa02\< 55 mmHg, PaC02\> 55 mmHg)
Primary Outcomes
Secondary Outcomes
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arteriel blood gas value (Pa02-mmHg) will be recorded before initiation of OLV and 30 minutes intervals up to 120 minutes after initiation of OLV and postoperative 1 hour. Pa02 in blood gas values will be recorded 20 minute after and 1 hour after arrival at postoperative care unit.
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Shunt fraction will be calculated with; Qs/Qt= (5,8xRI)+6,7 RI= Respiratory index RI= (PA02-Pa02)/ Pa02 PA02= Alveolar 02 pressure PA02= (\[PB-PH20\]x Fi02)- PaC02 PB= Atmosphere pressure= 760 mmHg PH20= Water vapor pressure= 47 mmHg shunt fraction will be recorded before initiation of OLV and 30 minutes intervals up to 120 minutes after initiation OLV
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Plato airway pressure (Pplato-mmHg) will be recorded before initiation of OLV and 30 minutes intervals up to 120 minutes after initiation of OLV. Change from initiation of Ppeak at 120 minute will be evaluated.
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arteriel blood gas value (PaC02-mmHg) will be recorded before initiation of OLV and 30 minutes intervals up to 120 minutes after initiation of OLV and postoperative 1 hour. PaC02 in blood gas values will be recorded 20 minute after and 1 hour after arrival at postoperative care unit.
More Details
NCT Number: | NCT02962999 |
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Other IDs: | KCOPD1 |
Study URL: | https://clinicaltrials.gov/study/NCT02962999 |