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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03876743
Other study ID # STU00206152
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 26, 2018
Est. completion date July 8, 2020

Study information

Verified date September 2020
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to determine if opiates are required to achieve adequate analgesia after knee arthroscopy and ACL reconstruction in outpatient surgery.

The investigators hypothesize that patients are frequently prescribed more opiates than are needed after surgery, resulting in excess medications that are at risk for misuse, diversion and contribution to the opioid epidemic.


Description:

Perioperative pain management is an important aspect of quality patient care. Opioid pain medications are increasingly being used for pain control, with the United States writing over 250 million prescriptions for painkillers per year. Increased usage has led to unintended negative consequences for individuals and society. It is estimated that 46 people die each day from an overdose of prescription painkillers, and individual use can lead to the development of tolerance and worse treatment outcomes. Further issues arise when opioids are misused, it is estimated that non-therapeutic use has increased three fold in recent years. In the United States alone in 2006 the estimated total cost of opioid prescription misuse was $53.4 billion, of which $42 billion was attributed to lost productivity, $8.2 billion to criminal justice cost and the remainder drug abuse treatment and medical complications. The federal government has recognized this epidemic and raised a call for clinicians to more responsibly prescribe opiate pain medications.

Opiate use has increased in recent years, from 2000-2010 the use of opiates in office based visits nearly doubled from 11.3% to 19.6% whereas there was no change in the prescribing of non-opioid pharmacotherapies. Further, when specifically looking at new musculoskeletal pain visits, one half resulted in pharmacologic treatment, with the prescribing of non-opioid pharmacotherapies decreasing from 38% to 29% from 2000 to 2010, respectively. The clinical use of opioids for post-operative pain control has also been linked to the opioid epidemic and risk of future abuse. Legitimate opioid use before high school graduation is independently associated with a 33% increased risk of future misuse after high school.

It has been estimated that orthopedic surgeons prescribe 7.7% of all opioids in the United States.Special attention needs to be paid to the amount of opioid pain medications orthopedic surgeons prescribe to patients after ambulatory surgery, there is considerable variability among surgeon and procedure in regards to the amount of opioids to prescribe with many patients left with excess unused medication.An analysis of 250 patients undergoing outpatient upper extremity surgery found that on average patients consumed 10 opioid pills, with 19 pills left over and a total of 4,639 pills going unused in the cohort. Leftover prescription opioids are at risk for diversion to family and friends for nonmedical use. Further studies are needed to quantify the amount of opioids to prescribe for specific orthopedic procedures to limit excess narcotic use, misuse, diversion and contribution to the opioid epidemic.


Recruitment information / eligibility

Status Completed
Enrollment 201
Est. completion date July 8, 2020
Est. primary completion date March 23, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 89 Years
Eligibility Inclusion Criteria:

- All patients presenting to Northwestern Memorial Hospital (NMH) or to a Northwestern orthopaedic surgery faculty member's clinic undergoing knee arthroscopy with meniscus repair and/or debridement

- 18 years old or greater

- Ability to read and speak English

Exclusion Criteria:

- Revision surgery

- Oncologic surgery

- Arthroscopic knee surgery that involves procedures other than ACL or the meniscus (i.e PCL, LCL, MPFL)

- Patients currently taking narcotics, chronic pain management patients, history of substance abuse

- Adults unable to consent

- Individuals who are not yet adults (infants, children, teenagers)

- Pregnant women

- Prisoners

- Patients currently taking narcotics, chronic pain management patients, history of substance abuse

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Group 1-Knee Arthroscopy
Will have all of their post-operative prescriptions sent down to the pharmacy on the day of surgery to be collected.
Group 2-Knee Arthroscopy
Will have all prescriptions sent to pharmacy with the exception of an opiate prescription. Instead, they will be handed a physical paper prescription. They will be instructed to only fill the prescription if absolutely needed.
Group 1-ACL reconstruction
Will be prescribed 60 opiate tablets in addition to other routine post-operative pain medication regimens.
Group 2-ACL reconstruction
Will be prescribed 30 opiate tablets in addition to other routine post-operative pain medication regimens.

Locations

Country Name City State
United States Northwestern Medicine Department of Orthopaedic Surgery Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numeric Pain Rating Scale (NPRS) Pain Score 2 hours post-op; minimum score: 0 = no pain, maximum score: 10 = worst imaginable pain; lower value is better 2 hours post-op
Primary Opiate Count 24 hours post-op 24 hours post-op
Primary Side Effects, 24 Hours Post-op Number of Participants with Side Effects, 24 hours post-op 24 hours post-op
Primary Numeric Pain Rating Scale (NPRS) Pain Scores 48 hours post-op; minimum score: 0 = no pain, maximum score: 10 = worst imaginable pain; lower value is better 48 hours post-op
Primary Opiate Count 48 hours post-op 48 hours post-op
Primary Side Effects 48 hours post-op 48 hours post-op
Primary Numeric Pain Rating Scale (NPRS) Pain Scores 7 days post-op; minimum score: 0 = no pain, maximum score: 10 = worst imaginable pain; lower value is better 7 days post-op
Primary Opiate Count Number Pills Taken 7 days post-op
Primary Number of Participants With Side Effects Potential side effects included lightheadedness, nausea, drowsiness, gastrointestinal symptoms, constipation 7 days post-op
Primary Refill Requests Number of participants requesting opioid refills within 3 months after surgery Within 3 months after surgery
Primary Still Taking Opiates? Number of patients who took any opiates between surgery and 1 day postoperative 1 day postoperative
Primary Still Taking Opiates? Number of patients who took any opiates between 1 day and 2 days postoperative 2 days postoperative
Primary Still Taking Opiates? Number of patients who took any opiates between 2 days and 7 days postoperative 7 days postoperatively
Primary Still Taking Opiates? Number of patients who took any opiates between 7 days and 21 days postoperative 21 days postoperatively
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