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Low Dose Naltrexone for Pain in Patients With HIV

Primary Purpose

Human Immunodeficiency Virus, Chronic Neuropathic Pain

Status
Suspended
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Low Dose Naltrexone
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Human Immunodeficiency Virus focused on measuring Low dose Naltrexone, Naltrexone, Pain

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-65, male and female
  • HIV infection with viral load of < 1000 copies/ml for the past six months. (That is viral load below which, according to the 2018 American College of Obstetricians and Gynecologists (ACOG) Committee Opinion, there is not thought to be a significant risk of HIV transmission from the mother to the fetus with vaginal delivery. This was thought to be a reasonable cut off for inclusion in this study.)
  • Diagnosis of neuropathic pain (pain that is associated with a lesion or disease involving the somatosensory nervous system, e.g. painful neuropathy, radicular pain, complex regional pain syndrome, nerve related pain following spine surgery, etc.)
  • Pain score > 4/10 on average on the NPRS lasting > 3 months (chronic pain)
  • Capable of informed consent and willingness to comply with the study requirements
  • Fluent English speaking

Exclusion Criteria:

  • Allergy to naltrexone
  • Current use of any opioids, excluding tramadol up to 1 week prior to the start of the study

  • Pregnant women, nursing mothers and women of childbearing potential not using contraception known to be highly effective. Highly effective contraception methods include combination of any two of the following during the 12 week study period: Low Dose Naltrexone for the Treatment of Chronic Neuropathic Pain in Patients with Human Immunodeficiency Virus (HIV), a Prospective, Pragmatic, Open Label Clinical Trial

    1. Use of oral, injected or implanted hormonal methods of contraception or;
    2. Placement of an intrauterine device (IUD) or intrauterine system (IUS);
    3. Barrier methods of contraception; condom or occlusive cap (diaphragm or cervical /vault caps) with spermicidal foam/gel/film/cream/vaginal suppository;
    4. Total abstinence;
    5. Male/female sterilization.
  • Bipolar disorder, schizophrenia, poorly controlled anxiety or depression
  • End-stage liver disease, e.g. cirrhosis
  • End-stage kidney disease, e.g. requiring chronic peritoneal or hemodialysis
  • Acute viral hepatitis A, B, C
  • Active drug or alcohol use disorder
  • People who may require opioid therapy during the duration of the study, e.g. upcoming surgery
  • Transportation issues interfering with return study visits (NA for the control group)
  • Adults unable to consent
  • Individuals who are not yet adults (infants, children, teenagers)
  • Prisoners
  • Cognitively impaired or Individuals with Impaired Decision-Making Capacity
  • Individuals who are not able to clearly understand English

Sites / Locations

  • Grady Memorial Hospital
  • Emory Midtown Hospital
  • Emory University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Low Dose Naloxone (LDN)

Arm Description

Once a potential subject has been identified they may be contacted with information about the study in advance of their appointment in order to allow time for them to consider the study. A qualifying pain score will be confirmed with the subject prior to initiating consent. This may occur up to 30 days before the baseline, treatment visit, but inclusion/exclusion criteria will be re-confirmed prior to initiating study treatment. Patients may also be approached during a clinic visit. Should a patient decline participation in the treatment plan, they will be invited to participate in a control group. They will be invited to complete the PROMIS questionnaire every 4 weeks, and the NPRS pain assessment every week from Baseline through week 12. These participants will receive follow up phone calls to confirm completion of these assessments weekly and will not have any in-person visits.

Once a potential subject has been identified they may be contacted with information about the study in advance of their appointment in order to allow time for them to consider the study. A qualifying pain score will be confirmed with the subject prior to initiating consent. This may occur up to 30 days before the baseline, treatment visit, but inclusion/exclusion criteria will be re-confirmed prior to initiating study treatment. Patients may also be approached during a clinic visit. Subjects will be started with 3mg LDN orally administered daily for one week with a planned increase to 4 mg/day beginning week two, if tolerated. They will be provided a 4 week supply of study medication. LDN will be given as a daytime dose.

Outcomes

Primary Outcome Measures

Changes in Numerical Pain Score
The study team will give participants a link to the online PROMIS questionnaire that includes a numerical pain rating scale (NPRS) to complete using an iPad or computer and will verbally ask questions to establish baseline information required for the study. If they have no computer access they will be given a hard copy of the PROMIS questionnaire and NPRS to complete for future visits. The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain). Changes in pain scores, measured on the numerical pain score (NPS) on the Pain Intensity section of the PROMIS-29 Profile v2.0. This will be measured weekly during the 12 week study period.
Changes in PROMIS pain Score
The study team will give participants a link to the online PROMIS questionnaire to complete using an iPad or computer and will verbally ask questions to establish baseline information required for the study. If they have no computer access they will be given a hard copy of the PROMIS questionnaire to complete for future visits. Changes on the overall score of the PROMIS-29 Profile v2.0 questionnaire collected at baseline, 4, 8 and 12 weeks will be assessed. The patients' answers to the PROMIS-29 are scored from 1-5. The sum of the PROMIS results in the raw score, which lies between 4 and 20. There is no total score, but each axis forms its own score. PROMIS assessments use an Item Response Theory (IRT) based score called "Expected A Posteriori" or EAP scores, which are then transformed onto a final T-score metric. The scores are mapped so that the values follow a normal distribution with a population mean T-score of 50 and a standard deviation of 10.
Changes in Average pain Score
The study team will give participants a link to the online PROMIS questionnaire that includes a numerical pain rating scale (NPRS) to complete using an iPad or computer and will verbally ask questions to establish baseline information required for the study. If they have no computer access they will be given a hard copy of the PROMIS questionnaire and NPRS to complete for future visits. The study team will compare the average weekly pain scores of the study group with the control group.

Secondary Outcome Measures

Changes in IL-1 levels
Blood will be drawn by phlebotomy services according to institutional practice. Samples for will be sent to the Emory Medical Laboratory at EUH or Emory University Hospital Midtown (EUHM) for processing and analysis. Serum cytokines values will be measured at the 12 week visit and will be compared to baseline visit values.
Changes in IL-6 levels
Blood will be drawn by phlebotomy services according to institutional practice. Samples for will be sent to the Emory Medical Laboratory at EUH or Emory University Hospital Midtown (EUHM) for processing and analysis. Serum cytokines values will be measured at the 12 week visit and will be compared to baseline visit values.
Changes in IL-8 levels
Blood will be drawn by phlebotomy services according to institutional practice. Samples for will be sent to the Emory Medical Laboratory at EUH or Emory University Hospital Midtown (EUHM) for processing and analysis. Serum cytokines values will be measured at the 12 week visit and will be compared to baseline visit values.
Changes in IL-18 levels
Blood will be drawn by phlebotomy services according to institutional practice. Samples for will be sent to the Emory Medical Laboratory at EUH or Emory University Hospital Midtown (EUHM) for processing and analysis. Serum cytokines values will be measured at the 12 week visit and will be compared to baseline visit values.
Changes in CRP Levels
Blood will be drawn and collected by phlebotomy services according to institutional practices into 2 purple top tubes (EDTA, 10 ml) at the baseline and 12 week visits. These samples will be sent to the Emory Research Hemostasis and Coagulation Core Laboratory (ERHCCL) Changes in C-reactive protein (CRP) levels at the 12 week visit compared to baseline visit levels.
Changes in TNF-α Levels
Blood will be drawn and collected by phlebotomy services according to institutional practices into 2 purple top tubes (EDTA, 10 ml) at the baseline and 12 week visits. These samples will be sent to the Emory Research Hemostasis and Coagulation Core Laboratory (ERHCCL) Changes in TNF-α levels at the 12 week visit compared to baseline visit levels.
Changes in Met-Encephalin Levels
Blood will be drawn and collected by phlebotomy services according to institutional practices into 2 purple top tubes (EDTA, 10 ml) at the baseline and 12 week visits. These samples will be sent to the Emory Research Hemostasis and Coagulation Core Laboratory (ERHCCL) Changes in Met-Enkephalin levels at the 12 week visit compared to baseline visit levels.
Changes in endorphin levels
Blood will be drawn and collected by phlebotomy services according to institutional practices into 2 purple top tubes (EDTA, 10 ml) at the baseline and 12 week visits. These samples will be sent to the Emory Research Hemostasis and Coagulation Core Laboratory (ERHCCL) Changes in endorphin levels at the 12 week visit compared to baseline visit levels.
Changes in DC4 counts
Blood will be drawn and collected by phlebotomy services according to institutional practices into 2 purple top tubes (EDTA, 10 ml) at the baseline and 12 week visits. These samples will be sent to the Emory Research Hemostasis and Coagulation Core Laboratory (ERHCCL) Changes in CD4 counts levels at the 12 week visit compared to baseline visit levels.

Full Information

First Posted
September 9, 2022
Last Updated
June 9, 2023
Sponsor
Emory University
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1. Study Identification

Unique Protocol Identification Number
NCT05537935
Brief Title
Low Dose Naltrexone for Pain in Patients With HIV
Official Title
Low Dose Naltrexone (LDN) for the Treatment of Chronic Neuropathic Pain in Patients With Human Immunodeficiency Virus (HIV), a Prospective, Pragmatic, Open Label Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Suspended
Why Stopped
Recruitment has been temporarily paused for IRB review
Study Start Date
April 28, 2023 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
March 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The increased life expectancy of Patients Living With HIV/AIDS (PLWHA) has increased the need for therapies for chronic conditions, such as chronic pain. Pain in the HIV population is often refractory and ends up being treated with chronic opioids, which are associated with adverse effects, including hyperalgesia, constipation, and risk of overdose. Naltrexone is an opioid antagonist used in the treatment of alcohol and opioid use disorders. Low Dose Naltrexone (LDN), naltrexone at a much lower dose, is thought to be an immune modulator and has been associated with an increased CD4 count in PLWHA. Repurposing this medication is relatively inexpensive, and has the potential to expand access to treatment for a painful condition experienced in PLWHA. While there are many case reports on the efficacy of LDN in symptom reduction, there are only a small number of clinical trials that specifically examine pain and symptom relief. This study will include patients who are not completely virologically controlled and will monitor the CD4 counts drawn as a part of routine care. If the CD4 count improves with LDN and with reduced symptoms, this could be a significant improvement in HIV therapy for symptom control. There have been studies showing cytokine reduction in fibromyalgia patients but they did not investigate the correlation with cytokines and pain relief. This study involves repurposing of a drug used for substance use disorder to a medication with the potential to treat pain and improve symptoms for PLWHA.
Detailed Description
More than one million people in the United States live with HIV. In 2018, Black/African Americans made up 42% of the new HIV diagnoses, while Hispanic persons accounted for 27%. Black/African Americans and Hispanics with an HIV diagnosis receive less care for treatment and maintenance of HIV than their Caucasian counterparts, and are thus less likely to have adequate suppression of the virus. Many people living with HIV/AIDS have untreated chronic pain which negatively affects their quality of life. Neuropathic (nerve) pain, including painful HIV neuropathy, is notoriously difficult to treat. Opioids (narcotics) are often used to treat chronic pain in patients, with inconsistent results. We now know that opioids for chronic pain are more consistently known for a multitude of side effects, than effective long-term pain relief. Lesser-known side effects of chronic opioids includes suppressing, or dampening, the immune system, making opioids particularly undesirable as a chronic therapy for pain in the HIV patient population. Other therapies for neuropathic pain have undesirable side effects. Naltrexone is FDA approved for addiction and is not used to treat a medical disease. Low-dose naltrexone (LDN) is an off-label use of naltrexone with some evidence it may help chronic pain such as fibromyalgia and some types of neuropathic (nerve) pain. LDN is a much lower dose of naltrexone. It has to be compounded to 1/10th the usual dose in order to be repurposed to treat pain. In this study, 40 adult patients with HIV will take low-dose naltrexone for 12 weeks to treat neuropathic pain. We will measure pain scores and markers of inflammation while they are taking LDN. Naltrexone repurposed as LDN has the potential to greatly enhance the quality of life of HIV patients. This is particularly meaningful given the healthcare disparities often associated with HIV.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Human Immunodeficiency Virus, Chronic Neuropathic Pain
Keywords
Low dose Naltrexone, Naltrexone, Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Once a potential subject has been identified they may be contacted with information about the study in advance of their appointment in order to allow time for them to consider the study. A qualifying pain score will be confirmed with the subject prior to initiating consent. This may occur up to 30 days before the baseline, treatment visit, but inclusion/exclusion criteria will be re-confirmed prior to initiating study treatment. Patients may also be approached during a clinic visit. Should a patient decline participation in the treatment plan, they will be invited to participate in a control group. They will be invited to complete the PROMIS questionnaire every 4 weeks, and the NPRS pain assessment every week from Baseline through week 12. These participants will receive follow up phone calls to confirm completion of these assessments weekly and will not have any in-person visits.
Arm Title
Low Dose Naloxone (LDN)
Arm Type
Experimental
Arm Description
Once a potential subject has been identified they may be contacted with information about the study in advance of their appointment in order to allow time for them to consider the study. A qualifying pain score will be confirmed with the subject prior to initiating consent. This may occur up to 30 days before the baseline, treatment visit, but inclusion/exclusion criteria will be re-confirmed prior to initiating study treatment. Patients may also be approached during a clinic visit. Subjects will be started with 3mg LDN orally administered daily for one week with a planned increase to 4 mg/day beginning week two, if tolerated. They will be provided a 4 week supply of study medication. LDN will be given as a daytime dose.
Intervention Type
Drug
Intervention Name(s)
Low Dose Naltrexone
Other Intervention Name(s)
Questionnaires
Intervention Description
Subjects will be started with 3mg LDN orally administered daily for one week with a planned increase to 4 mg/day beginning week two, if tolerated. They will be provided a 4 week supply of study medication. The most common side effects are difficulty sleeping and vivid dreams, which is seen more frequently with nighttime dosing, so LDN will be given as a daytime dose.
Primary Outcome Measure Information:
Title
Changes in Numerical Pain Score
Description
The study team will give participants a link to the online PROMIS questionnaire that includes a numerical pain rating scale (NPRS) to complete using an iPad or computer and will verbally ask questions to establish baseline information required for the study. If they have no computer access they will be given a hard copy of the PROMIS questionnaire and NPRS to complete for future visits. The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain). Changes in pain scores, measured on the numerical pain score (NPS) on the Pain Intensity section of the PROMIS-29 Profile v2.0. This will be measured weekly during the 12 week study period.
Time Frame
Study weeks 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,11 and 12
Title
Changes in PROMIS pain Score
Description
The study team will give participants a link to the online PROMIS questionnaire to complete using an iPad or computer and will verbally ask questions to establish baseline information required for the study. If they have no computer access they will be given a hard copy of the PROMIS questionnaire to complete for future visits. Changes on the overall score of the PROMIS-29 Profile v2.0 questionnaire collected at baseline, 4, 8 and 12 weeks will be assessed. The patients' answers to the PROMIS-29 are scored from 1-5. The sum of the PROMIS results in the raw score, which lies between 4 and 20. There is no total score, but each axis forms its own score. PROMIS assessments use an Item Response Theory (IRT) based score called "Expected A Posteriori" or EAP scores, which are then transformed onto a final T-score metric. The scores are mapped so that the values follow a normal distribution with a population mean T-score of 50 and a standard deviation of 10.
Time Frame
Study weeks 0, week 4, week 8 and week 12
Title
Changes in Average pain Score
Description
The study team will give participants a link to the online PROMIS questionnaire that includes a numerical pain rating scale (NPRS) to complete using an iPad or computer and will verbally ask questions to establish baseline information required for the study. If they have no computer access they will be given a hard copy of the PROMIS questionnaire and NPRS to complete for future visits. The study team will compare the average weekly pain scores of the study group with the control group.
Time Frame
Study weeks 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,11 and 12
Secondary Outcome Measure Information:
Title
Changes in IL-1 levels
Description
Blood will be drawn by phlebotomy services according to institutional practice. Samples for will be sent to the Emory Medical Laboratory at EUH or Emory University Hospital Midtown (EUHM) for processing and analysis. Serum cytokines values will be measured at the 12 week visit and will be compared to baseline visit values.
Time Frame
Study week 0 and week 12
Title
Changes in IL-6 levels
Description
Blood will be drawn by phlebotomy services according to institutional practice. Samples for will be sent to the Emory Medical Laboratory at EUH or Emory University Hospital Midtown (EUHM) for processing and analysis. Serum cytokines values will be measured at the 12 week visit and will be compared to baseline visit values.
Time Frame
Study week 0 and week 12
Title
Changes in IL-8 levels
Description
Blood will be drawn by phlebotomy services according to institutional practice. Samples for will be sent to the Emory Medical Laboratory at EUH or Emory University Hospital Midtown (EUHM) for processing and analysis. Serum cytokines values will be measured at the 12 week visit and will be compared to baseline visit values.
Time Frame
Study week 0 and week 12
Title
Changes in IL-18 levels
Description
Blood will be drawn by phlebotomy services according to institutional practice. Samples for will be sent to the Emory Medical Laboratory at EUH or Emory University Hospital Midtown (EUHM) for processing and analysis. Serum cytokines values will be measured at the 12 week visit and will be compared to baseline visit values.
Time Frame
Study week 0 and week 12
Title
Changes in CRP Levels
Description
Blood will be drawn and collected by phlebotomy services according to institutional practices into 2 purple top tubes (EDTA, 10 ml) at the baseline and 12 week visits. These samples will be sent to the Emory Research Hemostasis and Coagulation Core Laboratory (ERHCCL) Changes in C-reactive protein (CRP) levels at the 12 week visit compared to baseline visit levels.
Time Frame
Study week 0 and week 12
Title
Changes in TNF-α Levels
Description
Blood will be drawn and collected by phlebotomy services according to institutional practices into 2 purple top tubes (EDTA, 10 ml) at the baseline and 12 week visits. These samples will be sent to the Emory Research Hemostasis and Coagulation Core Laboratory (ERHCCL) Changes in TNF-α levels at the 12 week visit compared to baseline visit levels.
Time Frame
Study week 0 and week 12
Title
Changes in Met-Encephalin Levels
Description
Blood will be drawn and collected by phlebotomy services according to institutional practices into 2 purple top tubes (EDTA, 10 ml) at the baseline and 12 week visits. These samples will be sent to the Emory Research Hemostasis and Coagulation Core Laboratory (ERHCCL) Changes in Met-Enkephalin levels at the 12 week visit compared to baseline visit levels.
Time Frame
Study week 0 and week 12
Title
Changes in endorphin levels
Description
Blood will be drawn and collected by phlebotomy services according to institutional practices into 2 purple top tubes (EDTA, 10 ml) at the baseline and 12 week visits. These samples will be sent to the Emory Research Hemostasis and Coagulation Core Laboratory (ERHCCL) Changes in endorphin levels at the 12 week visit compared to baseline visit levels.
Time Frame
Study week 0 and week 12
Title
Changes in DC4 counts
Description
Blood will be drawn and collected by phlebotomy services according to institutional practices into 2 purple top tubes (EDTA, 10 ml) at the baseline and 12 week visits. These samples will be sent to the Emory Research Hemostasis and Coagulation Core Laboratory (ERHCCL) Changes in CD4 counts levels at the 12 week visit compared to baseline visit levels.
Time Frame
Study week 0 and week 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-65, male and female HIV infection with viral load of < 1000 copies/ml for the past six months. (That is viral load below which, according to the 2018 American College of Obstetricians and Gynecologists (ACOG) Committee Opinion, there is not thought to be a significant risk of HIV transmission from the mother to the fetus with vaginal delivery. This was thought to be a reasonable cut off for inclusion in this study.) Diagnosis of neuropathic pain (pain that is associated with a lesion or disease involving the somatosensory nervous system, e.g. painful neuropathy, radicular pain, complex regional pain syndrome, nerve related pain following spine surgery, etc.) Pain score > 4/10 on average on the NPRS lasting > 3 months (chronic pain) Capable of informed consent and willingness to comply with the study requirements Fluent English speaking Exclusion Criteria: Allergy to naltrexone Current use of any opioids, excluding tramadol up to 1 week prior to the start of the study Pregnant women, nursing mothers and women of childbearing potential not using contraception known to be highly effective. Highly effective contraception methods include combination of any two of the following during the 12 week study period: Low Dose Naltrexone for the Treatment of Chronic Neuropathic Pain in Patients with Human Immunodeficiency Virus (HIV), a Prospective, Pragmatic, Open Label Clinical Trial Use of oral, injected or implanted hormonal methods of contraception or; Placement of an intrauterine device (IUD) or intrauterine system (IUS); Barrier methods of contraception; condom or occlusive cap (diaphragm or cervical /vault caps) with spermicidal foam/gel/film/cream/vaginal suppository; Total abstinence; Male/female sterilization. Bipolar disorder, schizophrenia, poorly controlled anxiety or depression End-stage liver disease, e.g. cirrhosis End-stage kidney disease, e.g. requiring chronic peritoneal or hemodialysis Acute viral hepatitis A, B, C Active drug or alcohol use disorder People who may require opioid therapy during the duration of the study, e.g. upcoming surgery Transportation issues interfering with return study visits (NA for the control group) Adults unable to consent Individuals who are not yet adults (infants, children, teenagers) Prisoners Cognitively impaired or Individuals with Impaired Decision-Making Capacity Individuals who are not able to clearly understand English
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne M McKenzie-Brown, MD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Grady Memorial Hospital
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30303
Country
United States
Facility Name
Emory Midtown Hospital
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30308
Country
United States
Facility Name
Emory University Hospital
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported in this article, after deidentification (text, tables, figures, appendices)
IPD Sharing Time Frame
Beginning 3 months and ending 5 years following article publication
IPD Sharing Access Criteria
Data will be shared with researchers who provide a methodologically sound proposal, to achieve aims of the approved proposal. ? Proposals may be directed to amckenz@emory.edu. To gain access, data requestors will need to sign a data access agreement. Data are available 5 years at a 3rd party website

Learn more about this trial

Low Dose Naltrexone for Pain in Patients With HIV

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