Ireland
--:--IST
Starting soon Observational

Serum Bicarbonate Changes During Laparoscopic Bariatric Surgery

NCT07445230 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-03-01
Last updated
2026-03-03

Condition(s) studied

Acid Base Disorder

Investigational drug(s) / intervention(s)

Laparoscopic Bariatric Surgery

Laparoscopic Bariatric Surgery: Standard-of-care laparoscopic bariatric surgery (laparoscopic sleeve gastrectomy or Roux-en-Y gastric bypass) performed according to institutional protocols. No experimental intervention is introduced. The study prospectively observes perioperative serum bicarbonate changes and their association with pneumoperitoneum duration and early discharge readiness.

Study summary

Pneumoperitoneum during laparoscopic bariatric surgery induces carbon dioxide absorption and may lead to perioperative alterations in acid-base balance. Serum bicarbonate (HCO₃-) plays a central role in metabolic compensation; however, the clinical relevance of perioperative bicarbonate changes remains insufficiently defined.

This prospective observational study aims to evaluate the association between pneumoperitoneum duration and perioperative serum bicarbonate change (ΔHCO₃-), and to investigate whether ΔHCO₃- is associated with early discharge readiness at 48 hours (DR-48) following laparoscopic bariatric surgery. Patients undergoing laparoscopic sleeve gastrectomy or Roux-en-Y gastric bypass will be enrolled consecutively. No alteration of routine clinical care will occur.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults aged ≥18 years * ASA physical status I-III * Scheduled for elective laparoscopic bariatric surgery (laparoscopic sleeve gastrectomy or Roux-en-Y gastric bypass) * Provided written informed consent Exclusion Criteria: * Age \<18 years * ASA physical status IV or higher * Chronic obstructive pulmonary disease (COPD), asthma, or other severe chronic respiratory disease * Known chronic metabolic acidosis or renal failure * Major intraoperative complications (e.g., severe bleeding, conversion to open surgery) * Postoperative reoperation, intensive care requirement, or complications preventing standard recovery evaluation

Primary outcome measure(s)

  • Perioperative Serum Bicarbonate Change (ΔHCO₃-) — From baseline (after induction, before pneumoperitoneum) to 24 hours postoperatively
    Change in serum bicarbonate (HCO₃-) between the preoperative value (after induction, before pneumoperitoneum) and the postoperative 24-hour value, calculated as: ΔHCO₃- = HCO₃-(24 h postoperative) - HCO₃-(preoperative). The association between pneumoperitoneum duration (minutes) and ΔHCO₃- will be evaluated.

Trial sites (1)

FacilityCityRegionStatus
Istinye Üniversity Istanbul Merkez Mahallesi
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07445230 on ClinicalTrials.gov ↗ ← All trials in Turkey