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Completed

NCT Number: NCT00552682

Pilot, Opened, Randomized Clinical Trial to Assess the Efficacy of Duloxetine in the Treatment of Fibromialgy in Patients With Infection by HIV 1+

The purpose of this study is to compare duloxetine with conventional treatment of pain in HIV-1 infected patients.

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Key information

About this study

Among HIV-1-infected patients, diagnosis of fibromialgy has increased over the last years . Appropriate identification of firomialgy in these patients is challenging and sometimes can be more complicated than in HIV-negative population. Concomitant infectious processes and symptoms due to HIV infection itself need to be ruled out before establishing a formal diagnosis.

The treatment of this disease frequently includes muscular relaxants , pain-killers, anti-inflammatories and antidepressives despite no drug is formally indicated for this pathology.

Duloxetine approved indications include both treatment of major depressive disorders (MDD) and diabetic neuropathic pain. Recent studies in HIV negative patients show efficacy to control pain and depressive symptoms in patients with fibromialgy The main purpose of this pilot study is to assess the efficacy of duloxetine in HIV-1-infected patients with fibromialgy.

The main purpose of this pilot study is to assess the efficacy of duloxetine in HIV-1-infected patients with fibromialgy or chronic fatigue syndrome presenting with widespread pain.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged 18 years old and more. Age +18 years old.
  • Documented HIV-1-infection.
  • Former diagnosis of fibromialgy.
  • History of good compliance with visit schedule and medication intake.
  • Patients voluntary signed the informed consent.

Exclusion criteria

  • Pregnant or breast-feeding females
  • Suspicion of intolerance to duloxetine.
  • History of any clinical condition that, in the Investigator's criteria, could potentially reoccur with the suggested change of therapy (sarcoma, lymphoma, etc).
  • Concomitant condition that could mimic fibromialgy (lupus, endocrine diseases, muscular diseases, multiple sclerosis)
  • or Acute illness within 15 days prior to the inclusion
  • Patients with major depressive disorder with psychotic symptoms, major depressive disorder melancholic type or bipolar disorder. Patients with other depressive disorders can be included (dysthymic disorder and depressive disorder NOS)
  • Anorexia or nervous bulimia
  • History or suspected drug or alcohol abuse.
  • Glaucoma
  • History of heart disease including cardiac arrhythmias
  • Severe obesity (body mass index > 45).
  • Concomitant medication with IMAOS, cimetidine or quinolonas
  • Patients with hepatic or renal serious failure (Creatinin clearance <30 ml/min)
  • Patients with Hypericum perforatum as a concomitant treatment.

Treatment and study plan

Duloxetine 60 mg, QD

Drug

Duloxetine 60 mg, 1 table/day, 1 year

Other names: Xeristar

Primary outcomes

  1. Variation in pain measured using the Brief Pain Inventory questionnaire in both branches of the study

    Time frame: Time frame: basal visit, weeks 4, 12, 24, 36 and 48

Secondary outcomes

  1. Assess differences in Short-Form 36 Health Survey (SF-36) questionnaire scale score.

    Time frame: basal visit, weeks 12, 24 and 48

  2. Assess differences in Beck Depression Inventory (BDI) questionnaire scale score.

    Time frame: basal visit, weeks 12, 24 and 48

  3. Assess differences in Profile of Mood States - Forma A (POMS-A) questionnaire scale score.

    Time frame: basal visit, weeks 12, 24 and 48

  4. Assess the percentage of patients that leave duloxetine due to intolerance or toxicity.

    Time frame: basal visit, weeks 4, 12, 24, 36 and 48

  5. Assess, if possible, pharmacokinetic profile of duloxetine and determine interaction with antiretroviral drugs.

    Time frame: basal visit, weeks 4, 12, 24, 36 and 48

Sponsors and collaborators

Lead sponsor

Germans Trias i Pujol Hospital

Other

Collaborators

  • Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia

Registry information

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Nov 2, 2007
Registry last updated
Dec 4, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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