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Clinical Trials in Italy / NCT07591311
Recruiting Observational

The Quadro-Iliac Plane (QIP) Block in Hip Surgery

NCT07591311 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2026-05-04
Last updated
2026-09-02

Condition(s) studied

Hip SurgeryHip Arthroplasty

Investigational drug(s) / intervention(s)

Fascia iliaca block (FIB)

Fascia iliaca block (FIB): Fascia Iliaca Block

Study summary

The goal of this observational study is to learn about the effectiveness of different locoregional anesthesia techniques, particularly the Quadro-Iliac Plane (QIP) block, in patients undergoing hip surgery, including arthroplasty. The main question it aims to answer is:

Does the QIP block improve postoperative recovery and pain control compared to other routinely used locoregional anesthesia techniques in patients undergoing hip surgery?

Participants undergoing hip surgery as part of their standard clinical care will receive one of the locoregional anesthesia techniques already in use at the hospital (including QIP block, fascia iliaca block, PENG block, or others, according to anesthesiologist choice). Postoperative outcomes will be collected prospectively, including quality of recovery (QoR-15 at 24 hours), pain scores at rest and during movement at predefined time points up to 48 hours, analgesic consumption, time to first analgesic request, time to mobilization, and occurrence of complications.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years * Patients undergoing hip surgery, either elective or for a proximal femoral fracture * Expected postoperative hospital stay ≥ 24 hours * ASA physical status I-III * Neuraxial and/or locoregional anesthesia according to standard clinical practice * Provision of informed consent to participate in the study Exclusion Criteria: * Absence of informed consent * Contraindications to locoregional and/or spinal anesthesia * Allergy to local anesthetic agents * Cognitive impairment preventing reliable assessment of outcomes * Coagulation disorders and/or platelet abnormalities * Antiplatelet or anticoagulant therapy that contraindicates spinal anesthesia * Presence of localized infection or sepsis at the sites to be treated

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Crotone Hospital Crotone Italy Recruiting
Crotone Hospital Crotone Italy Recruiting

More San Giovanni di Dio Hospital trials in Italy

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 NCT07591311 on ClinicalTrials.gov ↗ ← All trials in Italy