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Atropine Weight and Risk of Postoperative Confusion in the Elderly (ATROPAGE)

T

Toulouse University Hospital

Status

Unknown

Conditions

Aging

Treatments

Other: Data collection

Study type

Observational

Funder types

Other

Identifiers

NCT03390751
RC31/17/0202
2017-A01847-46 (Registry Identifier)

Details and patient eligibility

About

The identification of a high atropine load of treatment received during hospitalization as a predictor of postoperative confusion could have various benefits:

  • Pharmacoepidemiological: identify factors associated with postoperative confusion
  • Clinics: by favoring treatments with a low atropine load during anesthesia, the management of patients hospitalized in orthopedics. Similarly, stopping or re-evaluating treatments with a high atropine weight for scheduled surgery is an easy step to take.
  • Socio-economic: by reducing the costs related to the occurrence of a confusional syndrome (over-treatment, prolonged hospital stay, loss of autonomy, institutionalization of patients...).

In total, the present study would improve the daily management of hospitalized patients and the practices of clinicians, by offering a decision-making aid.

Enrollment

130 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Admitted to the orthopedic department for surgical management of a fracture of the upper end of the femur in emergency or for the installation of a hip or knee prosthesis
  • Patient able to understand and respond to the protocol
  • No opposition to the collection of data of the patient or his / her designee

Exclusion criteria

  • Pre-existing confusion to surgery, detected by the CAM scale
  • Serious or moderate head trauma less than three months old
  • Removing / installing prosthesis.

Trial design

130 participants in 1 patient group

Aged patients
Description:
Data collection of patients admitted to the orthopedic department of the University Hospital of Toulouse for surgical management of a fracture of the upper end of the femur in emergency or for the installation of a hip or knee prosthesis.
Treatment:
Other: Data collection

Trial contacts and locations

1

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Central trial contact

Marie PIEL-JULIAN; Vincent Minville, MD PhD

Data sourced from clinicaltrials.gov

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