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Implementation of 23 Hour Surgery Model in a Tertiary Hospital (Herko)

K

Kuopio University Hospital

Status

Completed

Conditions

Ambulatory Surgery
Appendicitis
Ambulatory Surgical Procedures
Cholecystolithiasis
Laparoscopy
Ovarian Cysts
Neurosurgery
Gynecologic Surgical Procedures
Shoulder Impingement Syndrome

Treatments

Other: 23 h surgery

Study type

Observational

Funder types

Other

Identifiers

NCT04142203
KUH507A030

Details and patient eligibility

About

Extended day surgery or 23 h surgery (23-hour surgery) is a surgical model where patients arrive to the hospital from home at the day of surgery, are operated and recover in a 23 h surgery unit. 23H surgery units are usually situated near postoperative recovery unit. THe 23 H surgical model was implemented in Kuopio University Hospital 2015 and between May 2017-May 2018 patients were recruited in the present prospective follow up cohort study. Patients were informed and they gave their informed consent. The patients were contacted two weeks after the study and details of their recovery were asked.

Full description

Extended day surgery or 23 h surgery is a surgical model where patients arrive to the hospital from home at the day of surgery, are operated and recover in a 23 h surgery unit. 23H surgery units are usually situated near postoperative recovery unit. THe 23 H surgical model was implemented in Kuopio University Hospital 2015 and between May 2017-May 2018 patients were recruited in the present prospective follow up cohort study. Patients were informed and they gave their informed consent. The patients were contacted two weeks after the study and details of their recovery were asked. Satisfaction to the care in 23 h unit and surgical process, were asked. Amount of readmissions, reoperations, contacts to health care professionals and adverse events are recorded.

Detailed information about intensity of pain, analgesic need and use in the hospital was recorded and pain interference in daily life for short term recovery period was asked.

Enrollment

993 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • adult
  • gave informed consent

Exclusion criteria

  • no informed consent

Trial design

993 participants in 1 patient group

23 h surgery
Description:
Adult patients who were treated in 23 h surgical unit
Treatment:
Other: 23 h surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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