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Daycase Hip and Knee Arthroplasty in Møre and Romsdal Trial

Key facts

Who runs it
Helse Møre og Romsdal HF
Where
Ålesund, Hjelset, and Volda, NorwaySee the 3 sites
Trial code
Status
Not yet recruiting
People taking part
300 people, planned
Started
1 Oct 2026
Expected to end
31 Jul 2036
Type of study
Observational, 3 groups
Treatments tested
  • Total Hip Arthroplasty
  • Total Knee Arthroplasty
  • Unicondylar knee artrhoplasty
Record updated
22 September 2026

Who can take part

Age
18 years to 80 years
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 2 criteriaShow less

Who can take part

  • Patients 18-80 years old scheduled for primary TKA, UKA or THA

Who cannot take part

  • Patient not motivated for daycase surgery, lack of adult caregiver staying with the patient for the first 24 hours post-discharge, ASA class 3 (if not approved by anesthesiologist) and 4, travel distance to acute hospital no more than 1 hour (ferry-free), dementia or other reasons for lacking compliance (e.g. substance abuse, severe psychiatric disorder etc.) BMI >40 kg/m2, patients with anticipated high level of pain due to previous experience, comorbidity (i.e. chronic pain syndrome, fibromyalgia), patients treated with opoid analgesics on a regular basis prior to surgery

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Where in Norway

  • Ålesund sjukehusÅlesund, NorwayContact: Ole C Roth, MDNo longer taking part
  • Nordmøre and Romsdal Hospital (SNR) HjelsetHjelset, NorwayContact: Myrthle S Hoel, NurseNo longer taking part
  • Volda hospitalVolda, NorwayContact: Erik Ostnes, MDNo longer taking part

About the trial

What the trial wants to find out

The DART Study is a prospective, multicentre observational cohort study evaluating day-case pathways for patients undergoing primary total hip arthroplasty, total knee arthroplasty, or unicompartmental knee arthroplasty at three hospitals in Møre og Romsdal, Norway (Volda, Ålesund and SNR). All patients scheduled for these procedures will be screened for eligibility for same-day discharge using predefined clinical, functional, and logistical criteria.

Read full original descriptionShow less

The primary objective is to determine the proportion of patients who are discharged on the day of surgery. Secondary objectives are to assess recovery, pain, complications, emergency department visits, readmissions, reoperations, and mortality during the first 30 days after surgery. Patient-reported outcomes, including quality of recovery, joint-specific function, quality of life, pain, and awareness of the joint replacement, will be assessed before surgery and during follow-up for up to three months.

Clinical and patient-reported data will be collected prospectively. Outcomes for patients discharged on the day of surgery will be compared with those of patients who remain in hospital overnight or longer. The study aims to evaluate the feasibility, safety, and patient experience of implementing standardized day-case hip and knee arthroplasty pathways within routine clinical practice.

The 3 groups in the trial

  • Total Hip Arthroplasty

    Eligable patients for daycase surgery with hip osteoarthritis, osteonecrosis or other indication for total hip arthroplasty

  • Total Knee Arthroplasty

    Eligable patients for daycase surgery with knee osteoarthritis, osteonecrosis or other indication for total knee arthroplasty

  • Unicondylar Knee Arthroplasty

    Eligable patients for daycase surgery with knee osteoarthritis, osteonecrosis or other indication for unicondylar knee arthroplasty

    Treatment: Unicondylar knee artrhoplasty

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Fit questions
Built from NCT07834034, who can take part
Record updated
22 September 2026