Actively Recruiting

Age: 18Years +
All Genders
ID07072286

RELIEVED Study: Regional Anesthesia Techniques for Pain Management in Pelvic and Acetabular Fractures - A Prospective Pilot Cohort Study

Led by A.O.U. Città della Salute e della Scienza · Updated on 2025-07-18

200

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This observational study evaluates the impact of Regional Anesthesia (RA) techniques supported by anatomical and scientific evidence on managing acute post-operative pain in patients with pelvic or acetabular fractures. The study aims to find out if RA can reduce opioid use in the first 24 hours after surgery, decrease pain scores within 48 hours, and lower the incidence of complications and persistent post-surgical pain. Participants receive either RA techniques combined with standard multimodal analgesia or multimodal analgesia alone according to current clinical practice. RA methods include Supra-inguinal fascia iliaca block, lumbar erector spinae plane block, and transmuscular quadratus lumborum block, all performed by experienced anesthesiologists using ultrasound guidance and long-acting anesthetics. In cases where trained anesthesiologists are unavailable, patients receive only standard multimodal analgesic treatment. During and after surgery, researchers will assess pain intensity at scheduled times, track opioid use and side effects, and monitor the potential development of chronic pain. Functional recovery will be followed up clinically at 30, 60, and 90 days post-surgery. The main outcome measured is opioid consumption within 24 hours after surgery, along with secondary measures such as pain scores, opioid and RA side effects, and hospital stay length.

CONDITIONS

Brief Title

RELIEVED (REgionaL anesthesIa PElVic fracturEs stuDy) Study. Regional Anesthesia (RA) Techniques for Pain Management in Pelvic Fractures: A Prospective, Monocentric, Pilot Cohort Study.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older and able to provide informed consent
  • Patients with pelvic or acetabular fractures requiring surgery
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Absolute contraindications to regional anesthesia techniques such as uncorrectable bleeding disorders
  • Known allergy to local anesthetics
  • Technical inability to perform regional anesthesia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 48 hours after surgery

Participants receive regional anesthesia techniques or multimodal analgesia for pain management around the time of surgery for pelvic or acetabular fractures.

1 hospital stay including surgery and immediate post-operative care

Follow-up

Duration - Up to 90 days after surgery

Participants are monitored for pain scores, opioid consumption and side effects, persistent post-surgical pain, and hospital length of stay up to 90 days after surgery.

Visits at 6, 12, 24, 48 hours and at 30, 60, and 90 days post-surgery

Trial Site Locations

Total: 1 location

1

Centro Traumatologico Ortopedico (CTO) - AOU Città della Salute e della Scienza Univeristy Hospital

Turin, Italy, 10126

Actively Recruiting

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Research Team

M

Marco Ulla, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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