Open-label Milnacipran for Persistent Knee Pain One Year After Total Knee Arthroplasty (TKA)

Osteoarthritis Pain Clinical Trial

Official title:

Open-label Milnacipran for Persistent Knee Pain One Year After Total Knee Arthroplasty (TKA)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01780389
• Other study ID #: Pro00017445
• Secondary ID: SAV-MD-08
• Status: Completed
• Phase: Phase 4
• First received: January 29, 2013
• Last updated: January 20, 2015
• Start date: October 2010
• Est. completion date: July 2011

Study information

• Verified date: January 2015
• Source: Duke University
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug AdministrationUnited States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The current study examines the effects of milnacipran in patients who have chronic persistent knee pain one year or longer after total knee arthroplasty (TKA) to evaluate for a pain-relieving effect.

Description:

The current study proposes to collect pilot data on the utility of open-label milnacipran for the treatment of pain and other outcomes in this unfortunate group of patients with chronic persistent pain after TKA. Among marketed serotonin norepinephrine reuptake inhibitors (SNRIs), milnacipran has a unique property in that it blocks serotonin and norepinephrine reuptake equally. It is plausible that equipotent reuptake inhibition may confer greater analgesic benefit compared to other agents, and in preclinical animal models milnacipran has shown superior effects of ameliorating hyperalgesia and allodynia compared to some other antidepressant drugs. Additionally, milnacipran does not have inhibitory effects on cytochrome P (CYP) 450 enzymes, no binding affinity to neurotransmitter receptors liable to cause adverse events, and simple pharmacokinetics.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 5
• Est. completion date: July 2011
• Est. primary completion date: July 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subject is a male or female adult outpatient age 18 or older at the time of consent.

2. Subject has chronic persistent pain 1 year after TKA without history of new injury, infection, or implant failure.

3. Subject has VAS > or = 40 mm at screen and baseline visits.

4. Subject has an understanding, ability and willingness to fully comply with study procedures and restrictions.

5. Subject has the ability to provide written, personally signed and dated informed consent to participate in the study, in accordance with the International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) Guideline E6 and applicable regulations, before completing any study-related procedures.

Exclusion Criteria:

1. Subjects unable to complete assessments due to language or cognitive impairment

2. Subjects with a history of bipolar disorder or psychosis as confirmed by the Mini International Neuropsychiatric Interview (MINI).

3. Subject currently has (or had a history within the last 6 months of) a drug dependence or substance abuse disorder according to Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition Text Revision (DSM-IV-TR) criteria (excluding nicotine).

4. Subjects who are currently considered a suicide risk, any subject who has previously made a suicide attempt or who has a prior history of or are currently demonstrating active suicidal ideation.

5. Subject has any clinically significant ECG or clinically significant laboratory abnormality (including a positive urine drug screen) at Screening.

6. Subject has a concurrent chronic or acute illness, disability, or other condition that might confound the results of safety assessments administered in the study or that might increase risk to the subject. Similarly, the subject will be excluded if he or she has any additional condition(s) that in the Investigator's opinion would prohibit the subject from completing the study or would not be in the best interest of the subject. This would include any significant illness or unstable medical condition that could lead to difficulty complying with the protocol.

7. Subjects who do not agree to use adequate and reliable contraception throughout the study.

8. Subject previously completed, discontinued or was withdrawn from this study.

9. Subject has taken an investigational drug or taken part in a clinical trial within 30 days prior to Screening.

10. Subjects treated with antidepressant medication within 4 weeks of screening visit (6 weeks for fluoxetine).

11. Subjects with known sensitivity to milnacipran.

12. Subjects with liver disease or reduced liver function

13. Subjects with obstructive uropathies

14. Subjects who consume alcohol in amounts viewed by the Investigator to be contraindicated

15. Subjects taking monoamine oxidase inhibitors

16. Subjects with uncontrolled narrow angle glaucoma

17. Subjects who are pregnant, may become pregnant, or who are nursing

18. Subjects with seizure disorders

19. Subjects with bleeding disorders or use of other medications that may cause bleeding.

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Knee Pain After Total Knee Arthroplasty
• Osteoarthritis
• Osteoarthritis Pain

Intervention

Drug:
• Open-label flexibly dosed milnacipran

Locations

Country	Name	City	State
United States	Duke University Medical Center	Durham	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
Duke University

Country where clinical trial is conducted

United States, 

References & Publications (1)

Marks DM, Bolognesi MP. Open-label milnacipran for patients with persistent knee pain 1 year or longer after total knee arthroplasty: a pilot study. Prim Care Companion CNS Disord. 2013;15(4). pii: PCC.12m01496. doi: 10.4088/PCC.12m01496. Epub 2013 Jul 11 — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Pain Visual Analogue Scale(VAS).	The primary outcome is change in pain VAS from baseline to 12 weeks (baseline score minus 12 week or endpoint score; positive number reflects reduction in pain score). The effect size was calculated using the VAS scores measured on a scale of 0 to 100 mm: 0= absence of pain or no pain noted 100 = worst imaginable pain/as bad as can be The higher the score the greater the over all pain intensity.	baseline and endpoint 12 weeks	No
Secondary	Change in Knee Society Score (KSS).	KSS measures subjective pain and objective function by joint physical exam. This secondary outcome was the change in Knee Society Score(KSS)from baseline through 12 weeks.; KSS scores measured on a scale of 0 to 100 mm: 0 = absence of pain or no pain noted 100= worst imaginable pain/as bad as can be The higher the score the greater the over all pain intensity.	between baseline and endpoint (12 weeks or early termination)	No
Secondary	Global Rating of Change		Endpoint (12 weeks or early termination)	No
Secondary	Change in Total Score of Multidimensional Fatigue Inventory (MFI-20)	Measures subjective fatigue.20-item self-report instrument consisting of five scales: General Fatigue, Physical Fatigue, Reduced Activity, Reduced Motivation, and Mental Fatigue.; Each scale contains four items rated on a scale of one to 5 with the scale score of one having the anchor of entirely true and the scale score of 5 having the anchor of no, not true. The five scales were identified through factor analysis and are assumed to measure different aspects of fatigue. Lowest possible total score = 20 (absent fatigue) Highest possible total score = 100 (maximum fatigue) Total mean cumulative scores were reported	Baseline to endpoint (12 weeks or early termination)	No
Secondary	Change in the Beck Depression Inventory (BDI-II)	The secondary outcome measure is change in Beck Depression Inventory. The scale for this inventory is: 0-9: indicates minimal depression 10-18: indicates mild depression 19-29: indicates moderate depression 30-63: indicates severe depression. The higher the score the degree of depression.	Baseline to endpoint (12 weeks or early termination)	No
Secondary	Change in the Montgomery Asberg Depression Rating Scale	Staff-rated assessment of depressive symptoms. Scale is as follows: 0 to 6 - normal /symptom absent 7 to 19 - mild depression 20 to 34 - moderate depression >34 - severe depression	Between baseline and endpoint (12 weeks or early termination)	No
Secondary	Change in Total Score of State Trait Anxiety Inventory (STAI)	Assessment of subjective symptoms of current anxiety and chronic anxiety. There are 20 items for assessing trait anxiety and 20 for state anxiety. State anxiety items include: "I am tense; I am worried" and "I feel calm; I feel secure." Trait anxiety items include: "I worry too much over something that really doesn't matter" and "I am content; I am a steady person." All items are rated on a 4-point scale (e.g., from "Almost Never" to "Almost Always"). Higher scores indicate greater anxiety.; Lowest total score is 40 (absent anxiety) Highest total score is 160 (maximum anxiety) Total mean cumulative scores were reported.	baseline and endpoint (12 weeks or early termination)	No
Secondary	Change in Total Score of Short Form-36 (SF-36), Measuring Perceived Quality of Life	Subjective measure of perceived quality of life.The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight.; The eight sections are: vitality,; physical functioning,; bodily pain,; general health perceptions,; physical role functioning,; emotional role functioning,; social role functioning,; mental health; Scale: 0= lowest quality of life 100= high quality of life Higher scores reflect higher quality of life. Total mean cumulative scores were reported.	baseline and endpoint (12 weeks or early termination)	No