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Clinical Trials/NCT03219177
NCT03219177
Completed
Not Applicable

Patient Education and Use of Postoperative Pain Medication in Ambulatory Hand Surgery: a Randomized Controlled Trial

Hospital for Special Surgery, New York1 site in 1 country400 target enrollmentJune 15, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ambulatory Hand Surgery
Sponsor
Hospital for Special Surgery, New York
Enrollment
400
Locations
1
Primary Endpoint
Number of prescription opioids used postoperatively
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

There is a current opioid epidemic in the United States partially fueled by excess prescribing practices after surgery. The objective of this study is to decrease the amount of opioids needed after ambulatory hand surgery. In this randomized control trial, patients will be randomized into a patient education group and into a control group. The education group will be provided with a pre-operative video detailing proper indications for opioid use after hand surgery, alternative pain management strategies to try before using prescription opioid medications, and side effects associated with opioid use. Patients will also receive information on the current opioid epidemic. Patients will be reminded of the information given pre-operatively after surgery in the post-anesthesia care unit. The control group will not receive pre-operative education and will only receive standard of care post-operative counseling by nursing in the post-anesthesia care unit. All patients will be given a pain log, pain medication diary and participate in phone/email surveys to determine number of opioid pills taken, pain levels, and satisfaction with surgery. The investigators hypothesize that the education group will have decreased opioid intake and increased patient satisfaction compared to the control group.

Registry
clinicaltrials.gov
Start Date
June 15, 2017
End Date
December 6, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hospital for Special Surgery, New York
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • English Speaking: must be able to communicate over the phone or by email to perform questionnaires
  • Primary elective ambulatory hand surgery (bony or soft tissue)
  • Bony: Scaphoidectomy/ligament reconstruction tendon interposition (LRTI), Arthrodesis, Arthroplasty Soft Tissue: Carpal tunnel release (CTR), Trigger Finger (TF), DeQuervain's (DQ), Cyst removal, Cubital tunnel, Dupuytren's, tendon transfer, arthroscopy of wrist or elbow

Exclusion Criteria

  • Disability or preop pain in ipsilateral upper extremity from a secondary condition not related to the study procedure
  • Allergy or inability to consume oxycodone, Percocet or Vicodin due to a particular health state
  • Current Substance Abuse
  • HSS employees

Outcomes

Primary Outcomes

Number of prescription opioids used postoperatively

Time Frame: Within 14 days of surgery

Secondary Outcomes

  • Patient satisfaction(Post-op day 3, 8, and 15)
  • Pain level(Post-op day 3, 8, 15)
  • Surgical factors(Recorded on day of surgery)
  • Pain Catastrophization Score(Measured pre-operatively)
  • Mindfulness Attention Awareness Scale Score(Measured pre-operatively)
  • Adverse reactions to pain medication(Post-op day 3, 8, 15)
  • Prescriptions filled and refilled(Post-op day 3, 8, 15)
  • Alternative analgesia used(Post-op day 3, 8, 15)

Study Sites (1)

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