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Clinical Trials in Turkey / NCT07473583
Recruiting Observational

Pneumoperitoneum Duration and Bicarbonate Changes in Laparoscopic Hernia Surgery

NCT07473583 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-03-10
Last updated
2026-03-16

Condition(s) studied

Hernia, InguinalInguinal Hernia

Investigational drug(s) / intervention(s)

Laparoscopic Inguinal Hernia Repair (TAPP)

Laparoscopic Inguinal Hernia Repair (TAPP): Standard laparoscopic inguinal hernia repair performed using the transabdominal preperitoneal (TAPP) technique as part of routine clinical care. Pneumoperitoneum duration during the procedure will be recorded for analysis.

Study summary

The goal of this observational study is to learn how the length of pneumoperitoneum during laparoscopic inguinal hernia surgery may affect changes in blood bicarbonate levels. Pneumoperitoneum is the use of carbon dioxide gas to create space inside the abdomen during laparoscopic surgery.

The main question this study aims to answer is whether a longer pneumoperitoneum time is associated with changes in blood bicarbonate levels after surgery.

Participants are adults undergoing laparoscopic inguinal hernia repair as part of their routine medical care. Researchers will measure blood gas values, including bicarbonate levels, before surgery and again two hours after surgery. The change in bicarbonate levels will be compared with the duration of pneumoperitoneum during the operation.

The results of this study may help improve the understanding of metabolic changes that occur during laparoscopic surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years * Patients undergoing laparoscopic inguinal hernia repair using the TAPP technique * Ability to provide informed consent Exclusion Criteria: * Pregnancy * Severe cardiovascular disease * Renal insufficiency * Patients requiring additional intra-abdominal surgical procedures * Strangulated inguinal hernia requiring bowel resection

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Haseki Training and Research Hospital Istanbul Turkey (Türkiye) Recruiting

More Haseki Training and Research Hospital trials in Turkey

Other trials for the same condition

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 NCT07473583 on ClinicalTrials.gov ↗ ← All trials in Turkey