The Quadro-Iliac Plane (QIP) Block in Hip Arthroplasty
Recruiting now
Conditions studied: Hip Surgery, Hip Arthroplasty
In brief
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 total hip 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 replacement surgery? Participants undergoing hip arthroplasty 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.
Key facts
- Study ID
- NCT07591311
- Run by
- San Giovanni di Dio Hospital
- People needed
- 80
- Starts
- 2026-05-01
- Expected to finish
- 2027-11-01
- Last updated by the study team
- 2026-05-22
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 years
- Patients undergoing hip arthroplasty 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
You may not qualify if…
- 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
Where it is running
- Crotone Hospital — Crotone, Italy (enrolling)
- Crotone Hospital — Crotone, Italy (enrolling)
Full record on ClinicalTrials.gov
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