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Tracheal Colonization and Outcome After Major Abdominal Cancer Surgery

Tracheal Colonization and Outcome After Major Abdominal Cancer Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04002128
Enrollment
120
Registered
2019-06-28
Start date
2008-01-31
Completion date
2012-03-31
Last updated
2024-04-23

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

Conditions

Colorectal Neoplasms Malignant, Pancreatic Cancer, Adult, Stomach Neoplasms, Surgical Procedures, Operative

Keywords

tracheal colonization;, Bacteria;, Survival, Anesthesia, General;

Brief summary

The goals of this study were to investigate whether two anesthesia regimens, with and without N2O, and bacterial colonization influence respiratory complications after major abdominal surgery for cancer.

Detailed description

A study was approved by institutional ethics committee. All patients were informed on the study protocol by attending anesthesiologist on the day of the surgery and written informed consent was obtained. Patients with clinically or radiologically confirmed acute respiratory infections or those using antibiotics due to the respiratory infections a week prior to the surgery were not included in the study. Following risk factors were recorded in all patients: age, sex, weight loss in the last 6 months, comorbidities and operative time. Comorbidities were rated using ASA status and Charlson comorbidity index by 3 independent observers. Charlson comorbidity index was calculated after pathological examination. An advanced malignant disease was considered if tumor had infiltrated other organs or surrounding tissues, or when positive lymph nodes or metastases were confirmed. A group of 120 colorectal, gastric, or pancreatic cancer patients scheduled for surgery in the single centre were included in the prospective randomized study regardless of their ASA physical status. Nasopharyngeal smears were obtained in the preoperative area and tracheal aspirates were obtained in the operating room at the end of the surgery with a sterile suction catheter in a closed system. Postoperative Hgb; CRP and lung auscultation were done in all patients on the second and fourth postoperative day. Outcome measures registered were: * Postoperative pneumonia * Productive and difficult cough * Dysphonia * Congestive heart failure * postoperative complications, including hypertensive crisis, thromboembolic and infective complications were summarized one year after surgical treatment was finished & one year survival

Interventions

OTHERTracheal aspirates and nasal smears were taken in all the patients. Laparotomies were performed in all patients.

Nitrous oxyde and sevoflurane anesthesia may alter mucus transport in the early postoperative period. In colonized patients it may result in more respiratory complications.

Sponsors

Josip Juraj Strossmayer University of Osijek
CollaboratorOTHER
Osijek University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Masking description

Postoperative outcomes were registered by doctor who did not know type of anesthesia delivered

Intervention model description

To investigate whether productive cough, dyspnea and hoarseness were different between two groups of patients. Group Air received sevoflurane anesthesia with 35% O2 in air, and Group N2O received sevoflurane anesthesia with 35% O2 in N2O

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Adult patients diagnosis of gastric cancer, or colorectal cancer or pancreatic cancer * Scheduled for major abdominal surgery with organ resections * Written informed consent * Nasopharyngeal smears taken in the preoperative area * Tracheal aspirates taken at the end of the surgical procedure

Exclusion criteria

* Patients unable to understand study protocol and patients who refused study participation at any time * patients with clinically or radiologically confirmed acute respiratory infections at admission * antibiotic therapy due to the respiratory infections a week prior to the surgery

Design outcomes

Primary

MeasureTime frameDescription
Number of the patients with postoperative pneumoniaPostoperative day 4Number of patients who reported the presence of cough, dyspnea and/or abnormal findings on lung examination, and two of following: fever, leukocytosis or high CRP, and positive chest radiograms.
Number of the patients with productive cough and difficult expectorationPostoperative day 4patients without auscultatory findings who self reported that they have productive sputum and painful expectoration without laboratory and RTG findings suggestive for pneumonia
Number of the patients with hoarsenessPostoperative day 4The patients who self-reported hoarseness and changed voice

Secondary

MeasureTime frameDescription
One year survival and complicationsOne postoperative yearAll the other postoperative complications, including in-hospital hypertensive crisis, thromboembolic and infective complications were summarized one year after surgical treatment was finished.

Outcome results

None listed

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