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Treating Sexual Dysfunction From Selective Serotonin Reuptake Inhibitor (SSRI) Medication: a Study Comparing Requip CR to Placebo

Phase 4
Completed
Conditions
Sexual Dysfunction
Registration Number
NCT00334048
Lead Sponsor
St. Luke's-Roosevelt Hospital Center
Brief Summary

Antidepressant medicines sometimes cause sexual side effects. The purpose of this study is to determine whether the sexual dysfunction sometimes caused by selective serotonin reuptake inhibitor (SSRI) antidepressant medications can be reversed by treatment with Requip (ropinirole), a medicine which is used to treat Parkinson's Disease and restless leg syndrome.

Detailed Description

A significant proportion of patients taking pharmacotherapy for treatment of depression experience sexual dysfunction at distressing levels, with reported rates varying considerably. When sexual dysfunction is assessed prospectively using structured questionnaires, high levels of dysfunction have been found. SSRIs including paroxetine, sertraline, and other medications, have been shown to have a similar frequency of sexual side effects and in a recent prospectively designed study 50% of men taking sertraline reported that they were only "slightly" (18%) or "not at all" (32%) satisfied with their sexual functioning. It is reported that sexual side effects of antidepressant treatment frequently result in noncompliance with and/or premature discontinuation of treatment. A recent study showed that the dopamine agonist Requip (Ropinirole) reduced the amount of SSRI-associated sexual dysfunction. The proposed study will utilize a placebo control group in a crossover design to determine the effect on sexual dysfunction of adding Requip (Requip CR formulation) to the patient's SSRI treatment.

30 patients experiencing sexual dysfunction attributable to SSRI treatment for depression will be entered into this study. All patients will receive 6 weeks of treatment with Ropinirole and 6 weeks with placebo in a crossover fashion. Assessments of sexual functioning and depression will be made at each visit.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
9
Inclusion Criteria

  1. male or female outpatients 18-65 years old

  2. currently taking fluoxetine, sertraline, paroxetine, citalopram, or escitalopram at a stable dosage within the ranges specified for 1 month or longer required dosage range: (Prozac (fluoxetine) 20-80 mg/day; Celexa (citalopram) 20-60 mg/day; Lexapro (escitalopram) 10-30 mg/day; Zoloft (sertraline) 50-200 mg/day; Paxil (paroxetine) 20-60 mg/day; Paxil CR (paroxetine CR) 25-75 mg/day

  3. Currently responding to the SSRI antidepressant treatment, as indicated by

    • a score of 15 or less on the HDRS 24 item at screening and baseline, and (b) CGI-Severity score of 2 or less at baseline

  4. Meets DSM-IV criteria for Substance-Induced Sexual Dysfunction, with impairment of desire, arousal, or orgasm

  5. Are currently involved in an intimate relationship which includes sexual contact

  6. agree to use double-barrier contraception during sexual intercourse during the course of the study (women only)

  7. Agree to the study team contacting the physician who prescribe their SSRI medication to inform them of their participation in the current study

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Exclusion Criteria

  1. Patients with a DSM-IV diagnosis of Delirium, Dementia, and Amnestic, and other Cognitive Disorders,

  2. Patients with a principal diagnosis meeting DSM-IV criteria for: Bipolar Disorder or cyclothymia, Schizophrenia, Delusional (Paranoid) Disorders and Psychotic Disorders Not Otherwise Specified, or Anorexia Nervosa or Bulimia,

  3. Patients who, within the past 6 months, met DSM-IV criteria for abuse of or dependence on any drug, including alcohol,

  4. Patients who would pose a serious risk for suicide during the course of the study, as evidenced by one of the following:

    • report of having a specific plan for killing themselves,
    • a score of 3 or higher on the Hamilton Depression Rating Scale item 3 as rated by the study doctor at the first visit, (indicative of active suicidal thoughts or behaviors), or
    • a suicide attempt within the past 6 months,

  5. Patients with a history of medical conditions or procedures which may cause sexual dysfunction, including: peripheral vascular disease, radical prostatectomy, trans-urethral resection of the prostate [TURP], or spinal cord injury.

  6. History of sexual dysfunction predating onset of depression and/or initiation of antidepressant therapy,

  7. Patients receiving any other treatment for sexual dysfunction, including sex therapy

  8. Pregnant or nursing women.

  9. Patients with unstable or life-threatening medical conditions, such as uncontrolled hypertension, diabetes, or hypothyroidism, acute infections, pneumonia, severe renal or hepatic impairment.

  10. Patients with any the following: retinal disease, sleep apnea, or narcolepsy.

  11. Patients taking dopamine agonist medication.

  12. Patients taking medications that are

    • associated with orthostatic hypotension, such as tricyclic antidepressants, MAO Inhibitors, and alpha1 antagonists
    • CYP1A2 inhibitors, such as fluoroquinolones, fluvoxamine, cimetidine
    • SSRI medication used cyclically for PMDD

  13. Patients who do not expect to have regular sexual contact with another person over the next 13 weeks.

  14. Patients with a DSM-IV diagnosis of Pathological Gambling

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Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
International Index of Erectile Function (IIEF)6 weeks
Sexual Function and Satisfaction Questionnaire (SFSQ)6 weeks
Secondary Outcome Measures
NameTimeMethod
CGI-Sexual functioning (CGI-Sx)6 weeks
Hamilton Depression Rating Scale, 17 items (HDRS-17)6 weeks
Global Assessment of Functioning Scale (GAFS)6 weeks
Clinical Global Impressions (CGI)6 weeks

Trial Locations

Locations (1)

Mood Disorders Research Program

🇺🇸

New York, New York, United States

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