NCT02230657

Brief Summary

The purpose of this study is to identify differences in satisfaction, pain and length of stay between patients undergoing hip replacement who are discharged from the hospital on the day of surgery compared to patients who stay one night in the hospital.

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 29, 2014

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 3, 2014

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2015

Completed
Last Updated

October 21, 2015

Status Verified

October 1, 2015

First QC Date

August 29, 2014

Last Update Submit

October 20, 2015

Conditions

Osteoarthritis of the Hip

Outcome Measures

Primary Outcomes (1)

  • Patient Satisfaction

    Discharge through 30 days post-op

Study Arms (2)

Same day Discharge

ACTIVE COMPARATOR
Procedure: Same day discharge

Next day discharge

ACTIVE COMPARATOR
Procedure: Next day discharge

Interventions

Same day dischargePROCEDURE
Same day Discharge
Next day dischargePROCEDURE
Next day discharge

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Primary THA without acute hip fracture or prior hardware that would need to be removed at the time of surgery
  • Unilateral THA
  • Pre-operative Body Mass Index (BMI) \< 40 kg/m2
  • Age \< 75 years at time of surgery
  • Pre-operative hemoglobin \> 10 g/dL if pre-operative hemoglobin data is available
  • No history of cardiopulmonary disease that would necessitate inpatient monitoring after surgery
  • Pre-operative ambulatory status does not require the use of a walker or wheelchair
  • No chronic pre-operative opioid medication use or opioid addiction
  • Assistance available at home after discharge from hospital
  • No other condition or circumstance that would preclude rapid discharge from the hospital after surgery
  • Subject's English proficiency allows understanding of study and Informed Consent
  • Subject consented to participate in this study

You may not qualify if:

  • Revision THA
  • Bilateral THA
  • Pre-operative BMI ≥ 40 kg/m2
  • Age ≥ 75 at time of surgery
  • Pre-operative hemoglobin ≤ 10 g/dL if pre-operative hemoglobin data is available
  • History of cardiopulmonary disease requiring acute inpatient monitoring
  • Pre-operative ambulatory status requiring the use of a walker or wheelchair
  • Chronic pre-operative opioid medication use or opioid addiction
  • Limited or no assistance available at home after discharge from hospital
  • Any other condition or circumstance that would preclude rapid discharge from the hospital
  • Subject not proficient in English
  • Subject did not consent to participate in this study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Rothman Institute

Philadelphia, Pennsylvania, 19107, United States

Location

The Anderson Orthopaedic Clinic

Alexandria, Virginia, 22306, United States

Location

MeSH Terms

Conditions

Osteoarthritis, Hip

Condition Hierarchy (Ancestors)

OsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Study Design

Study Type
interventional
Phase
not applicable
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 29, 2014

First Posted

September 3, 2014

Primary Completion

August 1, 2015

Last Updated

October 21, 2015

Record last verified: 2015-10

Locations

US(2)