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Clinical Trials in Turkey / NCT07394816
Recruiting Observational

Can Ultrasound-Guided Fascial Plane Blocks Reduce Postoperative Pulmonary Complications After Major Abdominal Surgery?

NCT07394816 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-03-01
Last updated
2026-04-30

Condition(s) studied

Postoperative Pulmonary Complications (PPCs)Abdominal SurgeriesPostoperative Pain Management

Study summary

This prospective observational study aims to evaluate whether the use of ultrasound-guided fascial plane blocks is associated with a lower incidence of postoperative pulmonary complications in adult patients undergoing elective major abdominal surgery under general anesthesia.

Patients will be observed in two groups based on routine clinical practice: those who receive an ultrasound-guided fascial plane block for postoperative analgesia and those managed with other standard analgesic methods. The choice of analgesic technique will be determined by the responsible anesthesia team and not influenced by the study.

Postoperative pulmonary complications occurring within the first 7 days after surgery will be recorded using reopening the European Perioperative Clinical Outcome (EPCO) criteria. Secondary outcomes will include unplanned intensive care unit admission, length of hospital stay, and 30-day mortality. No additional procedures or interventions will be performed for research purposes.

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age 65 years or older * Scheduled for elective major abdominal surgery (e.g., colorectal, hepatobiliary, pancreatic, or gastric surgery) * ASA physical status II-III * Ability to provide written informed consent * Planned use of general anesthesia with or without adjunct regional techniques Exclusion Criteria: * Refusal or inability to provide informed consent * Known allergy or contraindication to local anesthetics * Coagulopathy or ongoing anticoagulant therapy contraindicating regional anesthesia * Infection at the site of planned block * Pre-existing chronic opioid use or chronic pain syndrome * Severe hepatic, renal, or cardiac failure (e.g., Child-Pugh C, end-stage renal disease, EF \<30%) * Cognitive impairment or severe dementia preventing adequate pain assessment * Emergency surgery * Body mass index (BMI \> 40 kg/m²)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Dr. Abdurrahman Yurtaslan Ankara Oncology Hospital Yenimahalle Ankara Recruiting

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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 NCT07394816 on ClinicalTrials.gov ↗ ← All trials in Turkey