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Clinical Trials in Italy / NCT07393139
Recruiting Observational

Early Postoperative Pain Following a Limb Amputation

NCT07393139 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2026-01-09
Last updated
2026-02-06

Condition(s) studied

Amputation, SurgicalPain ManagementRehabilitation

Investigational drug(s) / intervention(s)

Pain assessment

Pain assessment: During hospitalization, patients were asked three times daily to rate their pain using the 11 point NRS scale. The highest rating of each day will be extracted from their medical records.

Study summary

The primary aim of this study is to characterize the trajectory of pain and functional recovery in the first post-operative period following a limb amputation. Secondarily, this study aims to conduct an exploratory analysis to evaluate potential associations between clinical, demographical and therapeutical variables and primary outcomes including pain intensity, pain control and functional recovery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients ≥ 18 years of age * Patients who underwent an amputation to any limb, regardless of location or diagnosis Exclusion Criteria: * Patients with severe cognitive impairment or diagnosed with dementia * Patients deceased or in critical conditions within 48 hours of the intervention * Previous amputation to any limb * Admission to the hospital because of a stump revision

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
IRCCS Istituto Ortopedico Rizzoli Bologna Italy 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 NCT07393139 on ClinicalTrials.gov ↗ ← All trials in Italy