Efficacy of SNRI Treatment on Prefrontality in Patients With GAD and Other Comorbities

Phase 4

Completed

• Conditions: Generalized Anxiety Disorder
• Interventions: Drug: Desvenlafaxine

• Registration Number: NCT01975480
• Lead Sponsor: START Clinic for Mood and Anxiety Disorders

Brief Summary

This is an open-label flexible-dose pilot study evaluating the efficacy, safety, and tolerability of Pristiq (desvenlafaxine) in outpatient subjects diagnosed with Generalized Anxiety Disorder (GAD) with or without comorbidities that are secondary to the GAD. Primary trial objective is to evaluate the efficacy of Pristiq (desvenlafaxine) SNRI treatment 50 to 100 mg once daily in the treatment of GAD with or without comorbidities. Secondary trial objective is to determine whether or not treatment outcome in GAD is related to changes in cortical prefrontal activity of norepinephrine.

Detailed Description

Not available

Study Timeline

• Study Start: 2013-01
• Study First Submitted: 2013-10-23
• Study First Submitted QC: 2013-10-28
• Study First Posted: 2013-11-03
• Primary Completion: 2020-04-15
• Study Completion: 2020-05-01
• Status Verified: 2020-10
• Last Update Submitted: 2020-10-21
• Last Update Posted: 2020-10-23

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 29

Inclusion Criteria

• The patient has provided signed informed consent.
• Outpatients aged 18-65 (extremes included).
• Patients with a primary diagnosis of GAD according to DSM IV (300.23) criteria (diagnosis to be made using the Mini International Neuropsychiatric Interview; MINI Version 6.0.0). Patients with co-morbid anxiety disorders will be permitted, as long as GAD is judged to be the primary diagnosis.
• Patients who score a HAM-A of ≥ 20 at both Screening and Baseline, and ≥ 10 on the psychic and somatic anxiety factors.
• On the basis of physical examination, medical history, and basic laboratory screening, patient is, in the investigator's opinion, in a suitable condition.
• Willing and able to attend study appointments in the correct time windows.

Exclusion Criteria

• Any other axis I diagnosis that was a primary disorder in the previous six months.
• Alcohol or drug abuse as defined in the DSM IV (300.23) within the last six months.
• Mania, hypomania as defined in the DSM IV (300.23).
• Any psychotic disorder.
• Eating disorders as defined in the DSM IV (300.23).
• Any cognitive disorder or dementia within 3 months before the baseline visit.
• Clinical interpretation of apparent suicide risk.
• Continuation or commencement of formal psychotherapy.
• Current use of or commencement of antidepressant and anxiolytic medications.
• Failure on no more than 2 antidepressants (either SSRIs or SNRIs to exclude any treatment resistance.
• Patients, who have been on an antidepressant or other anxiolytic prior to the study, will have discontinued it more than two weeks prior to entry into the study. Those who have been on fluoxetine, will have been off of it for at least 5 weeks.
• Patients who have been on a herbal or alternative treatment judged to be potentially anxiolytic or with psychobiological activity (e.g. St. John's Wort, S-adenosylmethionine), will have terminated usage of the agent more than two weeks prior to entering the study.
• Scores on the Hamilton Depression Rating Scale (HAM-D) > 15, at screening visit 1
• Laboratory values at screening or in medical history that may be considered through clinical interpretation to be significant.
• Diseases that could through clinical interpretation interfere with the assessments of safety, tolerability and efficacy.
• Serious illness: Liver or renal insufficiency, cardiac, vascular, pulmonary, gastrointestinal, endocrine, neurological, infectious, neoplastic or metabolic disturbance.
• If female, the subject is pregnant or lactating or intending to become pregnant before, during or within 30 days after participating in this study; or intending to donate ova during such time period.
• The subject has received electroconvulsive therapy, vagal nerve stimulation, or repetitive transcranial magnetic stimulation within 6 months prior to Screening.
• The patient is, in the opinion of the investigator, unlikely to comply with the clinical trial protocol or is unsuitable for any reason.
• Known allergy or intolerance to desvenlafaxine or its excipients.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Desvenlafaxine	Desvenlafaxine	At the screening visit those who are eligible will enter a randomized trial with Pristiq (desvenlafaxine) 50 to 100 mg. The study will begin with a single week of Pristiq (desvenlafaxine) 50mg. Subsequently, tablets will be administered in a flexible dose fashion and patients will be followed up weekly (biweekly after week 8) and at the investigators discretion. After the first week the patients' dosage will be increased up to a maximum of 100 mg daily. This dose will remain fixed after 8 weeks of treatment until week 16.

Primary Outcome Measures

Name	Time	Method
Mean changes in the Hamilton Anxiety Rating Scale from baseline visit to week 16.	16 weeks

Secondary Outcome Measures

Name	Time	Method
Mean change from baseline to week 16 on the measures of prefrontality including: Frontal System Behavioural Scale and Behaviour Rating Inventory of Executive Function-Adult	16 weeks

Trial Locations

Locations (1)

START Clinic for Mood and Anxiety Disorders; 🇨🇦 Toronto, Ontario, Canada