Improving Pain and Reducing Opioid Use (IPaRO) in Lumbar Spine Surgery Patients

Lumbar Spinal Stenosis Clinical Trial

— IPaRO  

Official title:

Comparative Effectiveness of Multi-modal Pain Management Versus Standard Intra- and Post-operative Analgesia: Randomized Controlled Clinical Trial to Reduce Post-operative Pain and Opioid Use Among Patients Undergoing Lumbar Spine Surgery

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03088306
• Other study ID #: IRB00113816
• Status: Completed
• Phase: Early Phase 1
• Start date: July 1, 2017
• Est. completion date: August 31, 2018

Study information

• Verified date: October 2018
• Source: Johns Hopkins University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Patients presenting for lumbar spine surgery experience pain related to their spine condition. Following surgery, these patients also experience surgical pain resulting from disruption of skin, muscle tissue, vertebrae, intervertebral discs, and facet joints. This pain is often treated with opioid medications - with roughly 40% of patient experiencing sub-optimal pain management. Adequate pain control has become a top priority among professional societies, healthcare systems, and accrediting agencies. The current proposal will provide this critical evidence of feasibility and acceptability of a multi-modal pain management plan for patients undergoing lumbar spine surgery. Additionally, this study will provide critical preliminary data to compare the effectiveness of protocol-driven multi-modal pain management to control post-operative pain, reduce opioid medication use, and improve physical activity, sleep, and health.

Description:

Patients presenting for lumbar spine surgery experience pain related to their spine condition. Following surgery, these patients also experience surgical pain resulting from disruption of skin, muscle tissue, vertebrae, intervertebral discs, and facet joints. Proper pain management is necessary to reduce pain-related and medication side effects and to promote rehabilitation. This pain is often treated with opioid medications - with roughly 40% of patient experiencing sub-optimal pain management. Adequate pain control has become a top priority among professional societies, healthcare systems, and accrediting agencies.

Multi-modal pain management strategies have been proposed to (1) control pre-operative pain related to spine pathology; (2) employ non-opioid medication peri-operatively to pre-empt post-operative surgical pain; and (3) monitor and control pain intensity before and after surgery. There is a demonstrated lack of evidence regarding optimal post-operative protocols and pathways. The investigators have planned a randomized clinical trial to compare the effectiveness of two methods of peri-operative pain management to reduce post-operative pain and opioid use among patients undergoing lumbar spine surgery.

Prior to submission to National Institutes of Health (NIH), Agency for Healthcare Research and Quality (AHRQ), or Patient Centered Outcomes Research Institute (PCORI), it is necessary to demonstrate the feasibility and acceptability of the trial protocol. The current proposal will provide this critical evidence of feasibility and acceptability of a multi-modal pain management plan for patients undergoing lumbar spine surgery. Additionally, this study will provide critical preliminary data to compare the effectiveness of protocol-driven multi-modal pain management to control post-operative pain, reduce opioid medication use, and improve physical activity, sleep, and health.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 49
• Est. completion date: August 31, 2018
• Est. primary completion date: May 31, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 100 Years

Eligibility

Inclusion Criteria:

• Eligible participants will be English-speaking adults who are presenting to a spine surgeon (orthopaedic or neurosurgeon) for surgical treatment of a lumbar degenerative condition (spinal stenosis, spondylosis with or without myelopathy, and degenerative spondylolisthesis) using laminectomy with or without arthrodesis (i.e. fusion).

Exclusion Criteria:

• A microsurgical technique as the primary procedure, such as an isolated laminotomy or microdiscectomy.

• Spinal deformity as the primary indication for surgery.

• Spine surgery secondary to pseudarthrosis, trauma, infection, or tumor.

• Back and/or lower extremity pain < 3 months indicating no history of sub-acute or chronic pain.

• History of neurological disorder or disease, resulting in moderate to severe movement dysfunction.

• Presence of schizophrenia or other psychotic disorder.

• Patient refusal to participate.

• Known allergic reactions to any of the study medications

• Surgery under a workman's compensation claim.

• Not able to return to clinic for standard follow-up visits with surgeon.

• Unable to provide a stable address and access to a telephone.

Related Conditions & MeSH terms

• Lumbar Spinal Instability
• Lumbar Spinal Stenosis
• Lumbar Spine Degeneration
• Spinal Stenosis
• Spondylarthritis

Intervention

Drug:
• Standard analgesia use [Oxygen]
A protocol directed and clinically appropriate post-operative analgesia. In this study, standard post-operative analgesia is defined as: oxygen, volatile anesthesia, fentanyl, hydromorphone.
• Standard analgesia use [Hydromorphone]
A protocol directed and clinically appropriate post-operative analgesia. In this study, standard post-operative analgesia is defined as: oxygen, volatile anesthesia, fentanyl, hydromorphone.
• Standard analgesia use [Volatile Anesthesia]
A protocol directed and clinically appropriate post-operative analgesia. In this study, standard post-operative analgesia is defined as: oxygen, volatile anesthesia, fentanyl, hydromorphone.
• Standard analgesia use [Fentanyl]
A protocol directed and clinically appropriate post-operative analgesia. In this study, standard post-operative analgesia is defined as: oxygen, volatile anesthesia, fentanyl, hydromorphone.
• Multi-modal pain management [Acetaminophen + Gabapentin]
Administration of acetaminophen (1 gm po) plus gabapentin (600-1200 mg po) in the preparation area prior to surgery; pre-induction opioid titration with fentanyl until pain is relieved and/or respiratory depression ensues; intravenous ketamine (1 mg/kg load prior to incision then 10 mcg/kg/min) during surgery; acetaminophen, valium plus gabapentin during hospitalization; and prescription for acetaminophen, valium plus gabapentin at discharge.
• Multi-modal pain management [Fentanyl]
Administration of acetaminophen (1 gm po) plus gabapentin (600-1200 mg po) in the preparation area prior to surgery; pre-induction opioid titration with fentanyl until pain is relieved and/or respiratory depression ensues; intravenous ketamine (1 mg/kg load prior to incision then 10 mcg/kg/min) during surgery; acetaminophen, valium plus gabapentin during hospitalization; and prescription for acetaminophen, valium plus gabapentin at discharge.
• Multi-modal pain management [Intravenous Ketamine]
Administration of acetaminophen (1 gm po) plus gabapentin (600-1200 mg po) in the preparation area prior to surgery; pre-induction opioid titration with fentanyl until pain is relieved and/or respiratory depression ensues; intravenous ketamine (1 mg/kg load prior to incision then 10 mcg/kg/min) during surgery; acetaminophen, valium plus gabapentin during hospitalization; and prescription for acetaminophen, valium plus gabapentin at discharge.
• Multi-modal pain management [Valium + Gabapentin]
Administration of acetaminophen (1 gm po) plus gabapentin (600-1200 mg po) in the preparation area prior to surgery; pre-induction opioid titration with fentanyl until pain is relieved and/or respiratory depression ensues; intravenous ketamine (1 mg/kg load prior to incision then 10 mcg/kg/min) during surgery; acetaminophen, valium plus gabapentin during hospitalization; and prescription for acetaminophen, valium plus gabapentin at discharge.

Locations

Country	Name	City	State
United States	Johns Hopkins University School of Medicine	Baltimore	Maryland

Sponsors (2)

Lead Sponsor	Collaborator
Johns Hopkins University	North American Spine Society

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants undergoing lumbar spine surgery with complete follow-up	Number of participants undergoing lumbar spine surgery with complete follow-up	52 week
Secondary	Patient controlled analgesia (PCA) pump use	Total morphine equivalent of opioids administered by the PCA pump	during surgical hospitalization, up to 12 weeks
Secondary	Opioid medication use	How many patients were prescribed and using opioid medication over the 90 days after hospital discharge?	up to 90 days
Secondary	Patient Reported Outcomes Measurement Information System (PROMIS) Pain	Measure of pain intensity; Range 0 - 100; Population mean 50, standard deviation 10	at 6 and 12 weeks
Secondary	PROMIS Physical Function	Measure of physical function; Range 0 - 100; Population mean 50, standard deviation 10	at 6 and 12 weeks
Secondary	PROMIS Fatigue	Measure of fatigue; Range 0 - 100; Population mean 50, standard deviation 10	at 6 and 12 weeks
Secondary	PROMIS Anxiety	Measure of anxiety; Range 0 - 100; Population mean 50, standard deviation 10	at 6 and 12 weeks
Secondary	PROMIS Depression	Measure of depression; Range 0 - 100; Population mean 50, standard deviation 10	at 6 and 12 weeks
Secondary	PROMIS Sleep Disturbance	Measure of sleep disturbance; Range 0 - 100; Population mean 50, standard deviation 10	at 6 and 12 weeks
Secondary	PROMIS Satisfaction with Social Roles	Measure of satisfaction with social roles; Range 0 - 100; Population mean 50, standard deviation 10	at 6 and 12 weeks
Secondary	Health status (Medical Outcome Study Short Form 12, version 2)	Measure of physical and mental health; Range 0 - 100; Population mean 50, standard deviation 10	at 6 and 12 weeks
Secondary	Oswestry Disability Index (ODI)	Measure of pain-related disability; Range 0% - 100%; Scores greater than 30% indicative of moderate pain-related disability	at 6 and 12 weeks