M16.0 M16.1
Conditions
Interventions
Group 1: Study group:
- Training to walk with a support frame and crutches, including stairs, the evening before surgery
- Supplemental feeding with Nutricia preOp 200 ml, a drink rich in nutrients an
Sponsors
Hospital of Traumatology and Orthopaedics
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: • Elective unilateral total hip arthroplasty due to osteoarthritis • Age from 18 to 65 years • Moves without assistive devices • ASA 1-2 • BMI = 20-35.
Exclusion criteria
Exclusion criteria: • Refusal of the patient to participate in the study • The patient does not understand the essence of the study • Allergy to the medications included in the study • Addiction to opioid analgesics before surgery • Poorly compensated comorbidities • Blood coagulation disorders • After surgery, it is not possible to transfer the patient to the postoperative observation ward • Local complication during surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| number of days spent in hospital | — |
Secondary
| Measure | Time frame |
|---|---|
| - HOOS, JR scale – number of points 6 weeks after surgery and change in number of points from the initial state the day before surgery. - Satisfaction with treatment NRS from 0 to 10 on the day of discharge and 6 weeks after surgery. - Pain NRS at rest and during movement on the day of discharge and 6 weeks after surgery. - Morphine consumption on the day of surgery, on the first postoperative day, on the second postoperative day, and throughout the hospitalization period. | — |
Countries
Latvia
Contacts
Public ContactSergejs Zadoroznijs
Hospital of Traumatology and Orthopaedics / University of Latvia
Outcome results
None listed