Study of Placebo Without Deception Versus Standard Antidepressant for Major Depressive Disorder

NCT ID: NCT01650740

Last Updated: 2014-12-23

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 1 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-08-31
• Study Completion Date: 2014-11-30

Brief Summary

In recent years, there has been growing evidence that antidepressants are only marginally effective compared to placebo for mild to moderate depression. In other words, although many people improve when they take antidepressant medications, almost as many get better with placebo pills. One possible solution to this problem would be to give patients a trail of a placebo prior to giving them an antidepressant, however there are ethical issues with doing this deceptively. New evidence from other placebo-responsive disorders such as irritable bowel syndrome shows that people may benefit from placebos even if they know they are taking them. This study aims to determine whether giving placebos without deception to people with major depressive disorder followed by the option to switch to an antidepressant is an effective strategy. There will be 3 groups of subjects. The first group is a standard treatment arm and will receive duloxetine, an antidepressant. The second will be given a placebo with the option to switch to duloxetine if they do not improve. The third group will receive supportive clinical visits the option to switch to duloxetine if they do not improve. This design will allow us to determine whether a sequenced treatment of a placebo without deception and then the option to switch to an antidepressant is a viable strategy. It will also help us to determine to what degree the benefit comes from the ritual of receiving and taking the placebo tablet versus the benefit of visits with a doctor alone. The primary hypothesis is that there will be a less than 5% difference between response rates after 12 weeks in the sequenced placebo-then-antidepressant treatment group (both subjects who have remained on placebo as well as those who have switched to the antidepressant will be considered as one group) compared to the immediate antidepressant therapy group.

Conditions

Major Depressive Disorder

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Open-label duloxetine

12 week treatment with duloxetine

Group Type: EXPERIMENTAL

Duloxetine

Intervention Type: DRUG

30 mg daily x 1 week followed by 60 mg daily

Open-label Placebo

4 weeks of open label placebo with option to continue or switch to duloxetine for remaining 8 weeks.

Group Type: EXPERIMENTAL

placebo

Intervention Type: DRUG

small placebo capsule (30 mg duloxetine equivalent) x 1 week followed by 60 mg equivalent capsule daily

Supportive clinical management

4 weeks of supportive clinical management visits with option to continue or switch to duloxetine for remaining 8 weeks.

Group Type: EXPERIMENTAL

Study visits only

Intervention Type: OTHER

Weekly visits x 4 weeks followed by visits every 2 weeks

Interventions

Duloxetine

30 mg daily x 1 week followed by 60 mg daily

Intervention Type: DRUG

placebo

small placebo capsule (30 mg duloxetine equivalent) x 1 week followed by 60 mg equivalent capsule daily

Intervention Type: DRUG

Study visits only

Weekly visits x 4 weeks followed by visits every 2 weeks

Intervention Type: OTHER

Other Intervention Names

cymbalta

Eligibility Criteria

Inclusion Criteria

• Provision of written informed consent
• Diagnosis of major depressive disorder, currently depressed as determined by DSM-IV diagnostic criteria (confirmed using the MINI)
• Both females and males, aged 18 to 65 years
• Outpatient status
• Female patients of childbearing potential must have a negative urine human chorionic gonadotropin (hCG) test at enrolment and must be taking or willing to take some acceptable form of birth control during the course of the study if they are or plan to be sexually active
• A grade 8 English comprehension, the ability to understand and comply with the requirements of the study and capable of providing informed consent
• 17-item Hamilton Depression Rating Scale (HAM-D) score of 14-22 at screening and at baseline

Exclusion Criteria

• Diagnosis of a past hypomanic, manic or mixed state.
• Current or past psychotic symptoms
• Substance or alcohol dependence at enrolment (except dependence in full remission, and except for caffeine or nicotine dependence), as defined by DSM-IV criteria
• Opiates, amphetamine, barbiturate, cocaine, cannabis, or hallucinogen abuse by DSM-IV criteria within 4 weeks prior to enrolment
• Any pervasive developmental disorder (according to DSM-IV criteria)
• Diagnosis of dementia (according to DSM-IV criteria)
• Is at significant risk for suicide, as defined by a score of ≥ 2 on the suicide item of the MADRS, any suicidal ideation with intent or a plan within the 3 months prior to study entry or in the opinion of the investigator.
• Any history of lifetime suicide attempts
• Current treatment with an antidepressant medication
• Treatment with an antipsychotic, mood stabilizer or other psychoactive medication within a period of 5 half-lives of the medication prior to baseline visit
• Known intolerance, hypersensitivity or lack of response to duloxetine as judged by the investigator
• A history of treatment resistant depression (defined as 2 or more failed lifetime trials of antidepressant medication as judged by the investigator)
• Currently undergoing psychotherapy that was initiated within the past 3 months
• Significant medical condition that would contraindicate the use of duloxetine or that is untreated and would need urgent attention (as determined by treating physician)
• Medical conditions that would significantly affect absorption, distribution, metabolism, or excretion of duloxetine
• Unstable or inadequately treated medical illness (e.g. congestive heart failure, angina pectoris, hypertension) as judged by the investigator
• Any clinically significant deviation from the reference range in clinical laboratory test results as judged by the investigator
• Pregnancy (or female of child-bearing age not using adequate contraception) or lactation
• A positive β-hCG test at enrolment
• Involvement in the planning and conduct of the study
• Previous enrolment or randomisation of treatment in the present study
• Participation in another drug trial within 4 weeks prior enrolment into this study or longer in accordance with local requirements

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sunnybrook Health Sciences Centre

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Sunnybook Health Sciences Centre

Toronto, Ontario, Canada

Countries

Canada

Other Identifiers

081-2012

Identifier Type: -

Identifier Source: org_study_id