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

The Effect of Ultrasound-Guided Fascial Plane Blocks on Postoperative Pulmonary Complications in Patients Undergoing Major Abdominal Surgery: A Prospective Observational Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07394816
Acronym
FPB-PPC
Enrollment
500
Registered
2026-02-06
Start date
2026-03-01
Completion date
2026-08-15
Last updated
2026-04-30

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

Conditions

Abdominal Surgeries, Postoperative Pain Management, Postoperative Pulmonary Complications (PPCs)

Brief 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.

Interventions

None listed

Sponsors

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
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)

Design outcomes

Primary

MeasureTime frameDescription
Incidence of postoperative pulmonary complications (PPCs)Within the first 7 postoperative daysPostoperative pulmonary complications will be defined and recorded according to the European Perioperative Clinical Outcome (EPCO) criteria.

Countries

Turkey (Türkiye)

Contacts

CONTACTarif timuroglu
ariftimuroglu@yahoo.com+905072601980
PRINCIPAL_INVESTIGATORarif timuroglu

Dr. Abdurrahman yurtaslan Ankara Oncology Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 1, 2026