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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02107248
Other study ID # NL4670604413
Secondary ID P13-31 METC Twen
Status Completed
Phase N/A
First received
Last updated
Start date June 2014
Est. completion date March 2018

Study information

Verified date November 2018
Source Orthopedisch Centrum Oost Nederland
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim of the current study is to test the non-inferiority hypothesis of differences in early hip dislocation between a group of patients who will be restricted to sleep in supine position and a group without restricted sleeping position during the first eight weeks after a total hip replacement following a posterolateral surgical approach


Description:

stratified block randomized controlled trial


Recruitment information / eligibility

Status Completed
Enrollment 456
Est. completion date March 2018
Est. primary completion date March 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Placement of a primary total hip replacement via the posterolateral approach by a high volume orthopaedic surgeon

- Patients with a ASA-classification of I or II

Exclusion Criteria:

- Blindness

- Replacement of 2nd total hip within six months after the1st total hip replacement surgery

- Insufficient knowledge of the Dutch language

- Collum fracture

- Infection of total hip replacement

- Cognitive dysfunction

- Wheelchair dependability

- Hypermobility

- Alcohol abuse

- Neurological disorders such as Parkinson and stroke

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Sleep position: no restrictions
during the first eight weeks after total hip replacement following a posterolateral surgical approach
Sleep position: supine
during the first eight weeks after total hip replacement following a posterolateral surgical approach

Locations

Country Name City State
Netherlands Orthopedisch Centrum Oost Nederland Hengelo Overijssel

Sponsors (1)

Lead Sponsor Collaborator
Orthopedisch Centrum Oost Nederland

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Other Sleeping position preference necessary information for the stratification procedure baseline
Primary Percentage early hip dislocations in first eight weeks after THP
Secondary HOOS Hip Disability and Osteoarthritis Outcome Score eight weeks and six months post-operative
Secondary VHS Quality of Sleep eight weeks and six months post-operative
Secondary EQ-5D Quality of Life eight weeks and six months post-operative
Secondary VAS/NRS hip pain intensity eight weeks and six months post-operative
Secondary Compliance anti-dislocation instructions diary for patients to report their compliance with the set of anti-dislocation instructions, among which is the (daily) reporting of their sleeping position in bed at night eight weeks post-operative
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