Actively Recruiting

Age: 65Years +
All Genders
NCT07309575

Regional Versus General Anesthesia for Hip Fracture and Postoperative Oxygenation

Led by University of Lisbon · Updated on 2025-12-30

102

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

U

University of Lisbon

Lead Sponsor

N

Northern Lisbon Hospital Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

With this study, the investigators intend to measure oxygen saturation before and after hip surgery in the context of proximal femur fracture, comparing two types of anesthesia (general or spinal). The investigators also intend to study the effects of the two anesthetic techniques on sleep apnea, delirium, respiratory complications, and length of hospital stay. This is an observational study, in which oxygen is measured at the fingertip with a sensor and a bracelet, without any intervention, inconvenience, or discomfort for the participant. Data will be collected on: respiratory complications, sleep apnea, delirium, length of hospital stay, and survival. Data will be collected in the operating room and wards of Santa Maria Hospital, Lisbon, Portugal over a period of approximately 24 hours after the participant's operation. Information about participant's health and co-morbidities will be recorded. There will be no implication for the participants' clinical care, since the study measurements will not be sent to the health professionals in charge. The operation, recovery, and treatments will not be influenced at any time by participation in the study.

CONDITIONS

Official Title

Regional Versus General Anesthesia for Hip Fracture and Postoperative Oxygenation

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Hospital admission for hip fracture
  • Scheduled for hip fracture surgery
  • Age above 65 years, both genders
  • Capable of consent or consent by responsible person
Not Eligible

You will not qualify if you...

  • Hip fracture occurring during hospitalization (not present upon admission)
  • Patient refusal to participate

AI-Screening

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Trial Site Locations

Total: 1 location

1

Northern Lisbon Hospital Center

Lisbon, Lisbon District, Portugal, 1635

Actively Recruiting

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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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