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OpenTrials
Completed

NCT Number: NCT02230657

A Prospective, Randomized Trial Comparing Same Day Discharge and Overnight Hospital Stay Among Total Hip Arthroplasties Done by the Direct Anterior Approach

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rothman Institute, Philadelphia, Pennsylvania, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

Same day discharge

Procedure

Next day discharge

Procedure

Primary outcomes

  1. Patient Satisfaction

    Time frame: Discharge through 30 days post-op

Sponsors and collaborators

Lead sponsor

Rothman Institute Orthopaedics

Other

Collaborators

  • The Anderson Orthopaedic Clinic

Registry information

Important dates

Primary completion
2015
First posted
Sep 3, 2014
Registry last updated
Oct 21, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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