search
Back to results

Naloxone Education in Total Joint Patients

Primary Purpose

Opioid Use, Pain, Musculoskeletal, Surgery

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pre-hospital naloxone education
Sponsored by
Carilion Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Opioid Use focused on measuring naloxone, patient education, joint arthroplasty

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients and "primary support person" pairs in which
  • the patient is planning total or partial elective hip replacement at Carilion Roanoke Memorial Hospital OR
  • the patient is planning total or partial elective knee replacement at Carilion Roanoke Memorial Hospital OR
  • willingness to participate in study activities

Exclusion Criteria:

  • Age < 18 years
  • Pregnancy
  • Poor cognitive function
  • Poor English language skills
  • Inmate

Sites / Locations

  • Institute for Orthopedics and Neurosciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Naloxone education

Standard Education

Arm Description

These participants will receive a pre-hospital naloxone education module during their pre-operative joint class

These participants will receive the standard pre-hospital education including pain management and opioid safety, but will not specifically be given the new naloxone-education module in the pre-hospital setting

Outcomes

Primary Outcome Measures

"Readiness to Use Naloxone" assessed by survey and Opioid Overdose Knowledge Scale administration
This measure is expressed as a binary yes/no for each patient-support person pair. It can be assessed with the survey tool used at the patient's follow up appointment. The patient/ support person pair must satisfy each of the three following conditions. patient reports naloxone is present in the home (or carried with the patient) (assessed by Y/N question) the support person reports knowledge of and immediate access to the naloxone (assessed by Y/N question) the support person demonstrates competency for naloxone administration by scoring a passing mark on the modified Opioid Overdose Knowledge Scale (OOKS) (Williams et al. 2013). For our purposes, this will be a score greater than or equal to 34/45. If the three conditions are met, then the pair is assessed a "yes" score on "Readiness to Use Naloxone". If any condition is not met, then the pair is assessed a "no" score on "Readiness to Use Naloxone".

Secondary Outcome Measures

Correlation between indication for surgery (described by International Classification of Diseases 9/10 code) and "Readiness to Use Naloxone"
"Readiness to Use Naloxone" as described in our primary outcome measure will be used in the majority of our secondary outcomes. It functions as a binary variable. Indications for surgery are described by International Classification of Diseases 9/10, which are categorical variables with a uniform unit of measure. These codes are entered into the patient's electronic medical record by the patient's surgeon and would be retrieved by a study team member. Codes expected to be present in the study include: Musculoskeletal 16-Osteoarthritis of the Hip Musculoskeletal 17-Osteoarthritis of the Knee
Correlation between procedure (Current Procedural Terminology code) and "Readiness to Use Naloxone"
"Readiness to Use Naloxone" as described in our primary outcome measure will be used in the majority of our secondary outcomes. It functions as a binary variable. The operations that patients undergo are described by Current Procedural Terminology codes, which are categorical variables with a uniform unit of measure. These codes are entered into the patient's electronic medical record by the patient's surgeon and would be retrieved by a study team member. Codes expected to be present in the study include: 1005073- Arthroplasty, knee, condyle and plateau 27130 - Arthroplasty, acetabular and proximal femoral prosthetic replacement (total hip arthroplasty), with or without autograft or allograft
Correlation between patient comorbidities (described by International Classification of Diseases 9/10 code and "Readiness to Use Naloxone"
"Readiness to Use Naloxone" as described in our primary outcome measure will be used in the majority of our secondary outcomes. It functions as a binary variable. Comorbidities are other elements of a patient's health that are identified by their primary care physicians or other specialists. These comorbidities International Classification of Diseases 9/10, which are categorical variables with a uniform unit of measure. These codes are entered into the patient's electronic medical record by the patient's surgeon and would be retrieved by a study team member. Codes expected to be present in the study include: Musculoskeletal 16-Osteoarthritis of the Hip Musculoskeletal 17-Osteoarthritis of the Knee
correlation between patient age and "Readiness to Use Naloxone"
age (exploratory analysis)
correlation between patient sex and "Readiness to Use Naloxone"
sex (exploratory analysis)
correlation between patient race and "Readiness to Use Naloxone"
race (exploratory analysis)
correlation between patient ethnicity and "Readiness to Use Naloxone"
ethnicity (exploratory analysis)
correlation between patient household income and "Readiness to Use Naloxone"
household income (exploratory analysis)
Amount of opioid used at home
milligrams of morphine equivalents
Post-operative pain as measured by the Patient Reported Outcome Measurement Information System Pain Interference 6a assessments
Each question usually has five response options ranging in value from one to five. To find the total raw score for a short form with all questions answered, sum the values of the response to each question. For the adult 6-item form, the lowest possible raw score is 6; the highest possible raw score is 30 (see all short form scoring tables in Appendix 1). All questions must be answered in order to produce a valid score using the scoring tables. If a participant has skipped a question, use the HealthMeasures Scoring Service (https://www.assessmentcenter.net/ac_scoringservice) to generate a final score. Locate the applicable score conversion table in Appendix 1 and use this table to translate the total raw score into a T-score for each participant. The T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation (SD) of 10. Therefore, a person with a T-score of 40 is one SD below the mean.
Post-operative pain as measured by the Patient Reported Outcome Measurement Information System Pain Intensity 3a
Each question has five response options ranging in value from one to five. To find the total raw score for the short form, sum the values of the response to each question. The lowest possible raw score is 3; the highest possible raw score is 15. For most Patient-Reported Outcomes Measurement Information System instruments, a score of 50 is the average for the United States general population with a standard deviation of 10 because calibration testing was performed on a large sample of the general population. The T-score is provided with an error term (Standard Error or SE). The Standard Error is a statistical measure of variance and represents the "margin of error" for the T-score. Important: A higher Patient-Reported Outcomes Measurement Information System T-score represents more of the concept being measured.
High risk behavior as measured by the Patient Reported Outcome Measurement Information System Pain Medication Misuse assessment
Each question has five response options ranging in value from one to five. To find the total raw score for the short form, sum the values of the response to each question. For this instrument, the lowest possible raw score is 7; the highest possible raw score is 35. All questions must be answered in order to produce a valid score. For most Patient-Reported Outcomes Measurement Information System instruments, a score of 50 is the average for the United States general population with a standard deviation of 10 because calibration testing was performed on a large sample of the general population. The T-score is provided with an error term (Standard Error or SE). The Standard Error is a statistical measure of variance and represents the "margin of error" for the T-score.
Patient and caregiver knowledge
Opioid Overdose Knowledge Scale: The Opioid Overdose Knowledge Scale items use a 'yes/no or don't know'; or 'true/false or don't know' response format. Each correct answer scores one point. 'Don't know' and incorrectly marked responses (mistakes) are scored zero. Total score range: 0-45 points. OPIOID OVERDOSE KNOWLEDGE SCALE (OOKS): INSTRUCTIONS Total Score (45 items): One point if marked (33 Correct/True items): 1a, 1b, 1c, 1d, 1e, 1f, 1g, 1h, 1i, 2b, 2c, 2d, 2e, 2g, 2h, 3a, 3b, 3d, 3f, 3g, 3i, 3j, 4a, 5a, 5b, 5c, 6a, 7a, 8b, 9T, 11T, 12T, 14T One point if NOT marked (12 Incorrect/False items): 2a, 2f, 2i, 2j, 3c, 3e, 3h, 3k, 5d, 5e, 10F, 13F. You might chose to use the 'record into same variables' function of Statistical Package for the Social Sciences and inverse the values of these items.
Patient and caregiver attitude
Opioid Overdose Attitude Scale: SCORING The Opioid Overdose Attitude Scale is scored continuously using a 5-point Likert scale: completely disagree (1 point), disagree (2 points), unsure (3 points), agree (4 points) and completely agree (5 points). Reverse negative items: The following negative items need to be reversed before computing the total of scale points: 4, 6, 7, 9, 11, 15, 16, 17, 18, 23, 24, 25. You can use the 'record into same variables' OPIOID OVERDOSE ATTITUDES SCALE (OOAS): INSTRUCTIONS function of Statistical Package for the Social Sciences. Recode these items as: completely disagree (5 point), disagree (4 points), unsure (3 points), agree (2 points) and completely agree (1 points). Totals Scores: Once negative items have been reversed, add all items' points. The total scale points can range from 28 to 140 points.
Prescription fill rate
patient reports naloxone is present in the home (or carried with the patient)
Naloxone accessibility
"yes/no" answer to the question: "Do you know where naloxone is stored in the home and have immediate access to it in an emergency?"
Rescuer competence measured by modified Opioid Overdose Knowledge Scale Score (see outcome 14 for scoring)
the support person demonstrates competency for naloxone administration by scoring a passing mark (34/45) on the modified Opioid Overdose Knowledge Scale

Full Information

First Posted
October 7, 2019
Last Updated
April 27, 2021
Sponsor
Carilion Clinic
Collaborators
Virginia Polytechnic Institute and State University
search

1. Study Identification

Unique Protocol Identification Number
NCT04868552
Brief Title
Naloxone Education in Total Joint Patients
Official Title
The Effect of Universal Pre-hospital Naloxone Education on Patient and Family Safety, Attitudes and Experience in the Surgical Patient: a Prospective Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 2021 (Anticipated)
Primary Completion Date
June 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Carilion Clinic
Collaborators
Virginia Polytechnic Institute and State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study examines the efficacy of a brief pre-hospital naloxone education module added to the standard "Total Joint Class" curriculum on patient safety and experience. Participants will consist of 250 patient-and-support-person pairs. The primary outcome is "readiness to use" naloxone - a proxy for opioid overdose safety. Patient factors contributing to this primary outcome as well as the effect on patient attitude and experience will also be investigated.
Detailed Description
Opioids are powerful pain medications which currently serve a necessary role in recovery after knee or hip replacement surgery. However, opioids also pose a danger to both the patient and to other members of the household in the event of accidental overdose because they can cause respiratory depression and death. To minimize the risk of opioid overdose, patients are educated in appropriate use and storage of their medication. They are also provided with a prescription for naloxone. Naloxone is an emergency-use, potentially life-saving antidote to opioid pain medication. It can be sprayed into the nostrils of the opioid overdose victim by a non-medically trained bystander while waiting for the ambulance to arrive, and can make the difference between life and death for a child or adult. However, only about 30% of patients choose to fill their naloxone prescription when they go home from hospital after joint replacement surgery at Carilion Roanoke Memorial Hospital. The first purpose of this study is to evaluate whether teaching patients about opioid overdose and naloxone treatment influences whether patients fill their naloxone prescription and whether they can appropriately administer naloxone in the event of an overdose in the home. Additionally, this study will look at what factors, other than pre-surgery education, influence whether a patient fills their naloxone prescription or not. The resources available for opioid overdose prevention in the community are limited, and this study will help guide the effective use of those resources. The participants in this study will be patients who are planning hip or knee replacement surgery. They will enroll together with their primary support person. Two hundred and fifty patient and primary-support-person pairs will be enrolled prospectively over a 9-month period. All participant pairs will be randomized to receive either only the current three-hour pre-operative Joint Class (which is mandatory for all patients with their support person and includes education on opioids and pain management), or to receive, in addition, a new educational module. The new module will consist of a modified version of the REVIVE! Course, a course designed for people without prior medical training on the recognition of an opioid overdose and appropriate response including naloxone administration. Participants will be asked to complete an enrollment questionnaire prior to the educational intervention, a 2-week Recovery Journal (pain and medication diary) following surgery, and a follow-up questionnaire at the first post-operative visit, 2 weeks after surgery. Patients will also receive a short, 3-4 item questionnaire 6 months after surgery to collect data on the risk of long-term opioid use and the outcome of the naloxone in the home. Demographic and clinical data that is collected will be used to describe the study population and determine factors that act as barriers to effective opioid overdose reversal with naloxone in the home. This study will also examine the influence of education on the experience of the patient within the healthcare system, attitudes of patients towards opioids and naloxone, and patient safety. Standardized assessments that will be used to address these study questions include the Opioid Overdose Knowledge Scale (OOKS), the Opioid Overdose Attitude Scale (OOAS), and the PROMIS Pain Medication Misuse, Pain Intensity, and Pain Interference short forms. There are few studies that examine the influence of naloxone education for the layperson, so evidence in this field is limited. This study is unique in that it moves the conversation from the arena of chronic pain management and opioid addiction and focuses on the population of patients managing acute pain before and after surgical procedures. Outcomes of this research will help to direct prevention resources by answering very topical questions about the usefulness and effects of naloxone co-prescription with opioids for acute pain.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Use, Pain, Musculoskeletal, Surgery, Overdose of Opiate
Keywords
naloxone, patient education, joint arthroplasty

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
prospective randomized
Masking
Outcomes Assessor
Masking Description
investigators analyzing data will not know whether participants are in the intervention or no-intervention group
Allocation
Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Naloxone education
Arm Type
Experimental
Arm Description
These participants will receive a pre-hospital naloxone education module during their pre-operative joint class
Arm Title
Standard Education
Arm Type
No Intervention
Arm Description
These participants will receive the standard pre-hospital education including pain management and opioid safety, but will not specifically be given the new naloxone-education module in the pre-hospital setting
Intervention Type
Other
Intervention Name(s)
Pre-hospital naloxone education
Intervention Description
a 5-10 minute pre-hospital education module teaching patients and support persons how and when to administer naloxone
Primary Outcome Measure Information:
Title
"Readiness to Use Naloxone" assessed by survey and Opioid Overdose Knowledge Scale administration
Description
This measure is expressed as a binary yes/no for each patient-support person pair. It can be assessed with the survey tool used at the patient's follow up appointment. The patient/ support person pair must satisfy each of the three following conditions. patient reports naloxone is present in the home (or carried with the patient) (assessed by Y/N question) the support person reports knowledge of and immediate access to the naloxone (assessed by Y/N question) the support person demonstrates competency for naloxone administration by scoring a passing mark on the modified Opioid Overdose Knowledge Scale (OOKS) (Williams et al. 2013). For our purposes, this will be a score greater than or equal to 34/45. If the three conditions are met, then the pair is assessed a "yes" score on "Readiness to Use Naloxone". If any condition is not met, then the pair is assessed a "no" score on "Readiness to Use Naloxone".
Time Frame
approximately 2 weeks (from surgery to first follow-up visit)
Secondary Outcome Measure Information:
Title
Correlation between indication for surgery (described by International Classification of Diseases 9/10 code) and "Readiness to Use Naloxone"
Description
"Readiness to Use Naloxone" as described in our primary outcome measure will be used in the majority of our secondary outcomes. It functions as a binary variable. Indications for surgery are described by International Classification of Diseases 9/10, which are categorical variables with a uniform unit of measure. These codes are entered into the patient's electronic medical record by the patient's surgeon and would be retrieved by a study team member. Codes expected to be present in the study include: Musculoskeletal 16-Osteoarthritis of the Hip Musculoskeletal 17-Osteoarthritis of the Knee
Time Frame
2 months (time from study enrollment to first post-op visit)
Title
Correlation between procedure (Current Procedural Terminology code) and "Readiness to Use Naloxone"
Description
"Readiness to Use Naloxone" as described in our primary outcome measure will be used in the majority of our secondary outcomes. It functions as a binary variable. The operations that patients undergo are described by Current Procedural Terminology codes, which are categorical variables with a uniform unit of measure. These codes are entered into the patient's electronic medical record by the patient's surgeon and would be retrieved by a study team member. Codes expected to be present in the study include: 1005073- Arthroplasty, knee, condyle and plateau 27130 - Arthroplasty, acetabular and proximal femoral prosthetic replacement (total hip arthroplasty), with or without autograft or allograft
Time Frame
2 months (time from study enrollment to first post-op visit)
Title
Correlation between patient comorbidities (described by International Classification of Diseases 9/10 code and "Readiness to Use Naloxone"
Description
"Readiness to Use Naloxone" as described in our primary outcome measure will be used in the majority of our secondary outcomes. It functions as a binary variable. Comorbidities are other elements of a patient's health that are identified by their primary care physicians or other specialists. These comorbidities International Classification of Diseases 9/10, which are categorical variables with a uniform unit of measure. These codes are entered into the patient's electronic medical record by the patient's surgeon and would be retrieved by a study team member. Codes expected to be present in the study include: Musculoskeletal 16-Osteoarthritis of the Hip Musculoskeletal 17-Osteoarthritis of the Knee
Time Frame
2 months (time from study enrollment to first post-op visit)
Title
correlation between patient age and "Readiness to Use Naloxone"
Description
age (exploratory analysis)
Time Frame
2 months (time from study enrollment to first post-op visit)
Title
correlation between patient sex and "Readiness to Use Naloxone"
Description
sex (exploratory analysis)
Time Frame
2 months (time from study enrollment to first post-op visit)
Title
correlation between patient race and "Readiness to Use Naloxone"
Description
race (exploratory analysis)
Time Frame
2 months (time from study enrollment to first post-op visit)
Title
correlation between patient ethnicity and "Readiness to Use Naloxone"
Description
ethnicity (exploratory analysis)
Time Frame
2 months (time from study enrollment to first post-op visit)
Title
correlation between patient household income and "Readiness to Use Naloxone"
Description
household income (exploratory analysis)
Time Frame
2 months (time from study enrollment to first post-op visit)
Title
Amount of opioid used at home
Description
milligrams of morphine equivalents
Time Frame
7 months (time from enrollment to 6 month follow-up phone call)
Title
Post-operative pain as measured by the Patient Reported Outcome Measurement Information System Pain Interference 6a assessments
Description
Each question usually has five response options ranging in value from one to five. To find the total raw score for a short form with all questions answered, sum the values of the response to each question. For the adult 6-item form, the lowest possible raw score is 6; the highest possible raw score is 30 (see all short form scoring tables in Appendix 1). All questions must be answered in order to produce a valid score using the scoring tables. If a participant has skipped a question, use the HealthMeasures Scoring Service (https://www.assessmentcenter.net/ac_scoringservice) to generate a final score. Locate the applicable score conversion table in Appendix 1 and use this table to translate the total raw score into a T-score for each participant. The T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation (SD) of 10. Therefore, a person with a T-score of 40 is one SD below the mean.
Time Frame
7 months (time from enrollment to 6 month follow-up phone call)
Title
Post-operative pain as measured by the Patient Reported Outcome Measurement Information System Pain Intensity 3a
Description
Each question has five response options ranging in value from one to five. To find the total raw score for the short form, sum the values of the response to each question. The lowest possible raw score is 3; the highest possible raw score is 15. For most Patient-Reported Outcomes Measurement Information System instruments, a score of 50 is the average for the United States general population with a standard deviation of 10 because calibration testing was performed on a large sample of the general population. The T-score is provided with an error term (Standard Error or SE). The Standard Error is a statistical measure of variance and represents the "margin of error" for the T-score. Important: A higher Patient-Reported Outcomes Measurement Information System T-score represents more of the concept being measured.
Time Frame
7 months (time from enrollment to 6 month follow-up phone call)
Title
High risk behavior as measured by the Patient Reported Outcome Measurement Information System Pain Medication Misuse assessment
Description
Each question has five response options ranging in value from one to five. To find the total raw score for the short form, sum the values of the response to each question. For this instrument, the lowest possible raw score is 7; the highest possible raw score is 35. All questions must be answered in order to produce a valid score. For most Patient-Reported Outcomes Measurement Information System instruments, a score of 50 is the average for the United States general population with a standard deviation of 10 because calibration testing was performed on a large sample of the general population. The T-score is provided with an error term (Standard Error or SE). The Standard Error is a statistical measure of variance and represents the "margin of error" for the T-score.
Time Frame
7 months (time from enrollment to 6 month follow-up phone call)
Title
Patient and caregiver knowledge
Description
Opioid Overdose Knowledge Scale: The Opioid Overdose Knowledge Scale items use a 'yes/no or don't know'; or 'true/false or don't know' response format. Each correct answer scores one point. 'Don't know' and incorrectly marked responses (mistakes) are scored zero. Total score range: 0-45 points. OPIOID OVERDOSE KNOWLEDGE SCALE (OOKS): INSTRUCTIONS Total Score (45 items): One point if marked (33 Correct/True items): 1a, 1b, 1c, 1d, 1e, 1f, 1g, 1h, 1i, 2b, 2c, 2d, 2e, 2g, 2h, 3a, 3b, 3d, 3f, 3g, 3i, 3j, 4a, 5a, 5b, 5c, 6a, 7a, 8b, 9T, 11T, 12T, 14T One point if NOT marked (12 Incorrect/False items): 2a, 2f, 2i, 2j, 3c, 3e, 3h, 3k, 5d, 5e, 10F, 13F. You might chose to use the 'record into same variables' function of Statistical Package for the Social Sciences and inverse the values of these items.
Time Frame
7 months (time from enrollment to 6 month follow-up phone call)
Title
Patient and caregiver attitude
Description
Opioid Overdose Attitude Scale: SCORING The Opioid Overdose Attitude Scale is scored continuously using a 5-point Likert scale: completely disagree (1 point), disagree (2 points), unsure (3 points), agree (4 points) and completely agree (5 points). Reverse negative items: The following negative items need to be reversed before computing the total of scale points: 4, 6, 7, 9, 11, 15, 16, 17, 18, 23, 24, 25. You can use the 'record into same variables' OPIOID OVERDOSE ATTITUDES SCALE (OOAS): INSTRUCTIONS function of Statistical Package for the Social Sciences. Recode these items as: completely disagree (5 point), disagree (4 points), unsure (3 points), agree (2 points) and completely agree (1 points). Totals Scores: Once negative items have been reversed, add all items' points. The total scale points can range from 28 to 140 points.
Time Frame
7 months (time from enrollment to 6 month follow-up phone call)
Title
Prescription fill rate
Description
patient reports naloxone is present in the home (or carried with the patient)
Time Frame
approximately 2 weeks (from surgery to first follow-up visit)
Title
Naloxone accessibility
Description
"yes/no" answer to the question: "Do you know where naloxone is stored in the home and have immediate access to it in an emergency?"
Time Frame
approximately 2 weeks (from surgery to first follow-up visit)
Title
Rescuer competence measured by modified Opioid Overdose Knowledge Scale Score (see outcome 14 for scoring)
Description
the support person demonstrates competency for naloxone administration by scoring a passing mark (34/45) on the modified Opioid Overdose Knowledge Scale
Time Frame
approximately 2 weeks (from surgery to first follow-up visit)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients and "primary support person" pairs in which the patient is planning total or partial elective hip replacement at Carilion Roanoke Memorial Hospital OR the patient is planning total or partial elective knee replacement at Carilion Roanoke Memorial Hospital OR willingness to participate in study activities Exclusion Criteria: Age < 18 years Pregnancy Poor cognitive function Poor English language skills Inmate
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cassandra Mierisch, MD
Phone
540-510-6200
Email
crmierisch@carilionclinic.org
First Name & Middle Initial & Last Name or Official Title & Degree
Sarah F Smith, RN, BSN, MSN
Phone
540-512-1056
Email
sfsmith@carilionclinic.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cassandra Mierisch, MD
Organizational Affiliation
Carilion Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute for Orthopedics and Neurosciences
City
Roanoke
State/Province
Virginia
ZIP/Postal Code
24014
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Naloxone Education in Total Joint Patients

We'll reach out to this number within 24 hrs