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Effectiveness of Long-Term Versus Short-Term Treatment of Generalized Anxiety Disorder With Venlafaxine XR

Primary Purpose

Anxiety Disorders

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Venlafaxine XR
Placebo
Sponsored by
University of Pennsylvania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety Disorders focused on measuring Generalized Anxiety Disorder, Chronic Mediation Treatment, Double-Blind, Placebo Controlled, Venlafaxine XR, Relapse

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: GAD diagnosis by structured interview Hamilton Anxiety Scale score of 18 or MORE Clinical Global Impressions Severity Scale score of at least 4 Hamilton Depression Scale score of 18 or less Hamilton Depression Scale suicide item score less than 2 Use of an effective form of contraception throughout the study Exclusion Criteria: Hypersensitivity to venlafaxine XR History of seizures Episode of major depressive disorder in the previous 6 months History of any psychotic illness, bipolar disorder, or dementia Substance abuse and dependence during the past 6 months Other anxiety disorders with the exception of social phobia as long as GAD is primary Regular use of anxiolytics or antidepressants within 7 days of study onset Use of fluoxetine or monoamine oxidase inhibitors within 28 days of study onset (low dose usage of benzodiazepines will not prevent participation) Use of other psychotropic medication besides benzodiazepines during the study

Sites / Locations

  • University of Pennsylvania, 3535 Market Street, Suite 670

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Active Comparator

Placebo Comparator

Placebo Comparator

Arm Label

Open-Label Group

Double-Blind Drug Group

Double-Blind Placebo Group

Double-Blind Drug-After-Drug Group

Double-Blind Placebo-After-Drug Group

Double-Blind Placebo-After-Placebo Group

Arm Description

6-month randomized phase of Venlafaxine XR at a flexible dose of 75 - 225 mg/d

6-month randomized, double-blind phase of Venlafaxine XR at a flexible dose of 75 - 225 mg/d occurring between months 6 - 12 of the study

6-month randomized, double blind phase of placebo occurring between months 6 - 12 of the study

6-month randomized, double blind phase of Venlafaxine XR at a flexible dose of 75 - 225 mg/d occurring between months 13 - 19 of the study

6-month randomized, double blind phase of placebo occurring between months 13 - 19 of the study

6-month randomized, double blind phase of placebo occurring between months 13 - 19 of the study

Outcomes

Primary Outcome Measures

Hamilton Rating Scale for Anxiety
Hamilton Rating Scale for Anxiety - The assessment of anxiety states by rating Each item is scored on a scale of 0 (not present) to 4 (severe), with a total score range of 0-56, where <17 indicates mild severity, 18-24 mild to moderate severity and 25-30 moderate to severe.

Secondary Outcome Measures

Clinical Global Impressions, Severity of Illness
The CGI provides an overall clinician-determined summary measure that takes into account a knowledge of the patient's history, psychosocial circumstances, symptoms, behavior, and the impact of the symptoms on the patient's ability to function. The CGI is rated on the following seven-point scale: 1=normal, not at all ill; 2=borderline mentally ill; 3=mildly ill; 4=moderately ill; 5=markedly ill; 6=severely ill; 7=among the most extremely ill patients. Results of the "Placebo After Placebo" group in Phase 3 were not entered due to sample size limitations.

Full Information

First Posted
September 12, 2005
Last Updated
November 29, 2016
Sponsor
University of Pennsylvania
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00183274
Brief Title
Effectiveness of Long-Term Versus Short-Term Treatment of Generalized Anxiety Disorder With Venlafaxine XR
Official Title
Short-term Versus Long-term Treatment in Generalized Anxiety Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
September 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pennsylvania
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will assess the effectiveness of venlafaxine XR, randomized to either venlafaxine XR or placebo in preventing the relapse of generalized anxiety disorder after 6 months of treatment versus 12 months of treatment.
Detailed Description
Generalized anxiety disorder (GAD) is a highly prevalent, chronic psychiatric disorder. Despite the fact that GAD frequently demands prolonged treatment with medication, very little is known about the benefits of long-term treatment. GAD is characterized by 6 months or more of exaggerated worry and tension that is unfounded or much more severe than the normal anxiety most people experience. People with GAD are unable to relax and often suffer from insomnia. Venlafaxine XR, a drug used to treat depression, has been shown to be effective in the short-term treatment of GAD. However, its benefits over a course of more than 8 weeks have not been assessed. This study will evaluate the effectiveness of venlafaxine XR in treating GAD on a long-term basis and preventing the relapse of GAD after 6 months of treatment versus 12 months of treatment. Participants in this double-blind study will first receive 6 months of open-label treatment with venlafaxine XR. Upon completion of this initial phase, participants will be randomly assigned to either continue on venlafaxine XR or begin taking placebo. After 12 months, participants taking venlafaxine XR will be randomly assigned to continue on the drug or switch to placebo. Participants will have 22 study visits over at least 18 months. Follow-up visits will occur 24 months after enrollment. Relapse of GAD will be assessed with the Hamilton Anxiety Scale and Global Severity and Improvement Scale. A variety of methods, including questionnaires and standardized scales, will be used to assess secondary outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety Disorders
Keywords
Generalized Anxiety Disorder, Chronic Mediation Treatment, Double-Blind, Placebo Controlled, Venlafaxine XR, Relapse

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
268 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Open-Label Group
Arm Type
Active Comparator
Arm Description
6-month randomized phase of Venlafaxine XR at a flexible dose of 75 - 225 mg/d
Arm Title
Double-Blind Drug Group
Arm Type
Active Comparator
Arm Description
6-month randomized, double-blind phase of Venlafaxine XR at a flexible dose of 75 - 225 mg/d occurring between months 6 - 12 of the study
Arm Title
Double-Blind Placebo Group
Arm Type
Placebo Comparator
Arm Description
6-month randomized, double blind phase of placebo occurring between months 6 - 12 of the study
Arm Title
Double-Blind Drug-After-Drug Group
Arm Type
Active Comparator
Arm Description
6-month randomized, double blind phase of Venlafaxine XR at a flexible dose of 75 - 225 mg/d occurring between months 13 - 19 of the study
Arm Title
Double-Blind Placebo-After-Drug Group
Arm Type
Placebo Comparator
Arm Description
6-month randomized, double blind phase of placebo occurring between months 13 - 19 of the study
Arm Title
Double-Blind Placebo-After-Placebo Group
Arm Type
Placebo Comparator
Arm Description
6-month randomized, double blind phase of placebo occurring between months 13 - 19 of the study
Intervention Type
Drug
Intervention Name(s)
Venlafaxine XR
Other Intervention Name(s)
selective serotonin and norepinephrine reuptake inhibitors, Effexor, Effexor XR, Venlafaxine hydrochloride extended release, Trevilor, Lanvexin
Intervention Description
Six month intervention of Venlafaxine XR treatment with flexible range of 75 to 225 mg/d
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
six month intervention with placebo drug
Primary Outcome Measure Information:
Title
Hamilton Rating Scale for Anxiety
Description
Hamilton Rating Scale for Anxiety - The assessment of anxiety states by rating Each item is scored on a scale of 0 (not present) to 4 (severe), with a total score range of 0-56, where <17 indicates mild severity, 18-24 mild to moderate severity and 25-30 moderate to severe.
Time Frame
Measured at Months 6 (Open Label), 12 (Double-Blind), and 18 (Double-Blind Relapse)
Secondary Outcome Measure Information:
Title
Clinical Global Impressions, Severity of Illness
Description
The CGI provides an overall clinician-determined summary measure that takes into account a knowledge of the patient's history, psychosocial circumstances, symptoms, behavior, and the impact of the symptoms on the patient's ability to function. The CGI is rated on the following seven-point scale: 1=normal, not at all ill; 2=borderline mentally ill; 3=mildly ill; 4=moderately ill; 5=markedly ill; 6=severely ill; 7=among the most extremely ill patients. Results of the "Placebo After Placebo" group in Phase 3 were not entered due to sample size limitations.
Time Frame
Measured at Months 6 (Open Label), 12 (Double-Blind), 18 (Double-Blind, and 24 (Double-Blind Relapse)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: GAD diagnosis by structured interview Hamilton Anxiety Scale score of 18 or MORE Clinical Global Impressions Severity Scale score of at least 4 Hamilton Depression Scale score of 18 or less Hamilton Depression Scale suicide item score less than 2 Use of an effective form of contraception throughout the study Exclusion Criteria: Hypersensitivity to venlafaxine XR History of seizures Episode of major depressive disorder in the previous 6 months History of any psychotic illness, bipolar disorder, or dementia Substance abuse and dependence during the past 6 months Other anxiety disorders with the exception of social phobia as long as GAD is primary Regular use of anxiolytics or antidepressants within 7 days of study onset Use of fluoxetine or monoamine oxidase inhibitors within 28 days of study onset (low dose usage of benzodiazepines will not prevent participation) Use of other psychotropic medication besides benzodiazepines during the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karl Rickels, MD
Organizational Affiliation
University of Pennsylvania
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pennsylvania, 3535 Market Street, Suite 670
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104-3309
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24061331
Citation
Rickels K, Etemad B, Rynn MA, Lohoff FW, Mandos LA, Gallop R. Remission of generalized anxiety disorder after 6 months of open-label treatment with venlafaxine XR. Psychother Psychosom. 2013;82(6):363-71. doi: 10.1159/000351410. Epub 2013 Sep 20.
Results Reference
background
PubMed Identifier
21135327
Citation
Rickels K, Etemad B, Khalid-Khan S, Lohoff FW, Rynn MA, Gallop RJ. Time to relapse after 6 and 12 months' treatment of generalized anxiety disorder with venlafaxine extended release. Arch Gen Psychiatry. 2010 Dec;67(12):1274-81. doi: 10.1001/archgenpsychiatry.2010.170.
Results Reference
result
PubMed Identifier
28437668
Citation
Jung J, Tawa EA, Muench C, Rosen AD, Rickels K, Lohoff FW. Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder. Psychiatry Res. 2017 Aug;254:8-11. doi: 10.1016/j.psychres.2017.04.025. Epub 2017 Apr 14.
Results Reference
derived
PubMed Identifier
24723432
Citation
Saung WT, Narasimhan S, Lohoff FW. Lack of influence of DAT1 and DRD2 gene variants on antidepressant response in generalized anxiety disorder. Hum Psychopharmacol. 2014 Jul;29(4):316-21. doi: 10.1002/hup.2404. Epub 2014 Apr 10.
Results Reference
derived
PubMed Identifier
23972788
Citation
Cooper AJ, Narasimhan S, Rickels K, Lohoff FW. Genetic polymorphisms in the PACAP and PAC1 receptor genes and treatment response to venlafaxine XR in generalized anxiety disorder. Psychiatry Res. 2013 Dec 30;210(3):1299-300. doi: 10.1016/j.psychres.2013.07.038. Epub 2013 Aug 22.
Results Reference
derived
PubMed Identifier
23658070
Citation
Cooper AJ, Rickels K, Lohoff FW. Association analysis between the A118G polymorphism in the OPRM1 gene and treatment response to venlafaxine XR in generalized anxiety disorder. Hum Psychopharmacol. 2013 May;28(3):258-62. doi: 10.1002/hup.2317. Epub 2013 May 8.
Results Reference
derived
PubMed Identifier
22907732
Citation
Lohoff FW, Narasimhan S, Rickels K. Interaction between polymorphisms in serotonin transporter (SLC6A4) and serotonin receptor 2A (HTR2A) genes predict treatment response to venlafaxine XR in generalized anxiety disorder. Pharmacogenomics J. 2013 Oct;13(5):464-9. doi: 10.1038/tpj.2012.33. Epub 2012 Aug 21.
Results Reference
derived
PubMed Identifier
22417933
Citation
Narasimhan S, Aquino TD, Multani PK, Rickels K, Lohoff FW. Variation in the catechol-O-methyltransferase (COMT) gene and treatment response to venlafaxine XR in generalized anxiety disorder. Psychiatry Res. 2012 Jun 30;198(1):112-5. doi: 10.1016/j.psychres.2011.12.034. Epub 2012 Mar 13.
Results Reference
derived
PubMed Identifier
22006095
Citation
Lohoff FW, Aquino TD, Narasimhan S, Multani PK, Etemad B, Rickels K. Serotonin receptor 2A (HTR2A) gene polymorphism predicts treatment response to venlafaxine XR in generalized anxiety disorder. Pharmacogenomics J. 2013 Feb;13(1):21-6. doi: 10.1038/tpj.2011.47. Epub 2011 Oct 18.
Results Reference
derived
PubMed Identifier
21889574
Citation
Narasimhan S, Aquino TD, Hodge R, Rickels K, Lohoff FW. Association analysis between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and treatment response to venlafaxine XR in generalized anxiety disorder. Neurosci Lett. 2011 Oct 10;503(3):200-2. doi: 10.1016/j.neulet.2011.08.035. Epub 2011 Aug 26.
Results Reference
derived

Learn more about this trial

Effectiveness of Long-Term Versus Short-Term Treatment of Generalized Anxiety Disorder With Venlafaxine XR

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