NCT07230704Completed
Effects of Low-Flow and Standard-Flow Sevoflurane Anesthesia on Inflammatory Markers in Bariatric Surgery
Effects of Low-Flow and Standard-Flow Sevoflurane Anesthesia on Perioperative Inflammation in Bariatric Surgery
Source: ClinicalTrials.gov · Last updated 27 Aug 2026
Brief summary (registry, in English)
This retrospective observational study aimed to compare the effects of low-flow and standard-flow sevoflurane anesthesia on perioperative inflammatory responses in patients undergoing laparoscopic sleeve gastrectomy for obesity. Data were obtained from the anesthesia and laboratory records of 155 adult patients who received either low-flow (1 L/min) or standard-flow (4 L/min) sevoflurane anesthesia between January 2022 and January 2025 at Adana City Training and Research Hospital. Preoperative and postoperative inflammatory markers, including C-reactive protein (CRP), neutrophil-to-lymphocyte ratio (NLR), and red cell distribution width (RDW), were recorded and compared between the two groups. Hemodynamic parameters such as mean arterial pressure and heart rate were also analyzed to assess intraoperative stability. The primary objective of the study was to evaluate the impact of anesthetic flow rate on perioperative inflammation, while the secondary objective was to assess hemodynamic stability during anesthesia. This study may contribute to a better understanding of how low-flow anesthesia influences systemic inflammatory responses and perioperative hemodynamics in morbidly obese patients undergoing bariatric surgery.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 155 (actual)
- First submitted
- 13 Nov 2025
- Start date
- 1 Jan 2022
- Primary completion date
- 31 Jan 2025
- Lead sponsor
- Adana City Training and Research Hospital
- Diseases
- Obesity
- NCT number
- NCT07230704
What you commit to
- Study type: Observational
- Participants enrolled: 155
- From 1 Jan 2022 to the primary completion date, 31 Jan 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Conversion to open surgery
Other illness
- Significant comorbidities (e.g., severe cardiac, hepatic, or renal dysfunction)
Age
- Age \<18 or \>60 years
Other
- Incomplete or missing data
- Perioperative complications unrelated to anesthesia
Who the study is looking for
- Adult patients aged 18-60 years
- Underwent laparoscopic sleeve gastrectomy under general anesthesia
- Received low-flow or standard-flow sevoflurane anesthesia
- ASA physical status I-III
- Complete perioperative records available
Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Adana City Training and Research Hospital Coordinator of this site? Confirm its status | Adana | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.