Page last updated: 2024-10-25

citalopram and Body Dysmorphic Disorders

citalopram has been researched along with Body Dysmorphic Disorders in 2 studies

Citalopram: A furancarbonitrile that is one of the serotonin uptake inhibitors used as an antidepressant. The drug is also effective in reducing ethanol uptake in alcoholics and is used in depressed patients who also suffer from TARDIVE DYSKINESIA in preference to tricyclic antidepressants, which aggravate dyskinesia.
citalopram : A racemate comprising equimolar amounts of (R)-citalopram and its enantiomer, escitalopram. It is used as an antidepressant, although only escitalopram is active.
1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-2-benzofuran-5-carbonitrile : A nitrile that is 1,3-dihydro-2-benzofuran-5-carbonitrile in which one of the hydrogens at position 1 is replaced by a p-fluorophenyl group, while the other is replaced by a 3-(dimethylamino)propyl group.

Body Dysmorphic Disorders: Preoccupations with appearance or self-image causing significant distress or impairment in important areas of functioning.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fang, A1
Porth, R1
Phillips, KA2
Wilhelm, S2
Keshaviah, A1
Dougherty, DD1
Stout, RL1
Menard, W1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Pharmacotherapy Relapse Prevention in Body Dysmorphic Disorder[NCT00149799]Phase 3100 participants (Actual)Interventional2005-05-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Phase I Response to Escitalopram (as Measured by the BDD-YBOCS)

We calculated the proportion of patients who achieved response in Phase I, defined as a >=30% reduction in BDD-YBOCS total score from baseline through the last phase 1 visit. (NCT00149799)
Timeframe: Phase I: Weekly for weeks 1-4, biweekly from weeks 6-14

Interventionpercentage of subjects who responded (Number)
Phase I: Open-Label Escitalopram67

Phase II Relapse of Body Dysmorphic Disorder (BDD) Symptoms (as Measured by the BDD-YBOCS)

We compared the rate of relapse (accounting for time from randomization to relapse and censoring) by treatment arm in Phase II. (NCT00149799)
Timeframe: Phase II: Biweekly for six months after randomization

Interventionpercentage of subjects who relapsed (Number)
Phase II: Escitalopram18
Phase II: Placebo40

Change in Depression Symptoms (HAM-D) During the Double-blind Relapse Prevention Phase of the Trial (Phase II)

Depressive symptoms were assessed with the Hamilton Rating Scale for Depression (HAM-D), a widely used 21-item depression scale. Of the 21 items on the scale, only the first 17 are used to calculate the total score. Eight of these items are scored on a 5-point scale, ranging from 0 (not present) to 4 (severe symptom), and nine are scored from 0-2. The total score ranges from 0 to 50, where higher scores indicate a greater severity of depression and scores greater than 19 are generally considered indicative of severe depression. (NCT00149799)
Timeframe: Measured bi-weekly in phase 2 from week 14 (start of randomization for relapse prevention) to week 40

,
Interventionunits on a scale (Mean)
Week 14Week 16Week 18Week 20Week 22Week 24Week 26Week 28Week 30Week 32Week 34Week 36Week 38Week 40
Phase II: Escitalopram3.53571433.89285715.28571434.84615384.23076923.6253.86956524.482.852.95652173.3754.04166673.81818184.2400000
Phase II: Placebo3.37931034.23333336.37037045.42857143.74074073.77272734.044.40909094.54545454.24.75.43.46666674.1578947

Change in Functional Impairment Symptoms (LIFE-RIFT) Over Double-blind Relapse Prevention Phase of the Trial (Phase II)

Subjects switched to placebo were compared to those remaining on escitalopram (double-blind randomization) to assess functional impairment as measured by the Longitudinal Interval Followup Evaluation - Range of Impaired Functioning Tool (LIFE-RIFT). The tool assesses psychosocial functioning in multiple domains, consisting of 5- to 7-point clinician administered scales that obtain information about work, household duties, student work, relationships with family and friends, recreation, life satisfaction, and global social adjustment. Scores can range from 3-22 with higher scores indicating poorer functioning. (NCT00149799)
Timeframe: Measured three times throughout phase 2 of study (Weeks 14, 28 and 40)

,
Interventionunits on a scale (Mean)
Week 14Week 28Week 40
Phase II: Escitalopram9.00000009.80000009.7600000
Phase II: Placebo8.24137939.00000008.8947368

Change in Quality of Life (Q-LES-Q-SF) Over Double-blind Relapse Prevention Phase of the Trial (Phase II)

Subjects switched to placebo were compared to those remaining on escitalopram (double-blinded randomization) to assess quality of life changes as measured by the Quality of Life Enjoyment and Satisfaction Questionnaire - Short Form (Q-LES-Q-SF). The Q-LES-Q-SF is designed to help assess the degree of enjoyment and satisfaction experienced during the past week across several domains: social, leisure, household, work, emotional well-being, physical, and school; it consists of 5-point rater-administered questions. Raw scores can range from 14-70, which are converted to percentage maximum possible by calculating: % Max = (Raw-minimum score)/(maximum score-minimum score). Q-LES_Q-SF percent scores can range from 0-100, with higher scores indicating greater quality of life and satisfaction. (NCT00149799)
Timeframe: Measured three times throughout phase 2 of study (Weeks 14, 28 and 40)

,
InterventionPercentage score (Mean)
Week 14Week 28Week 40
Phase II: Escitalopram74.178571470.272727369.0833333
Phase II: Placebo70.925925967.368421168.6470588

Trials

2 trials available for citalopram and Body Dysmorphic Disorders

ArticleYear
Personality as a Predictor of Treatment Response to Escitalopram in Adults With Body Dysmorphic Disorder.
    Journal of psychiatric practice, 2019, Volume: 25, Issue:5

    Topics: Adult; Body Dysmorphic Disorders; Citalopram; Drug Monitoring; Female; Humans; Male; Neuroticism; Ou

2019
Pharmacotherapy Relapse Prevention in Body Dysmorphic Disorder: A Double-Blind, Placebo-Controlled Trial.
    The American journal of psychiatry, 2016, Sep-01, Volume: 173, Issue:9

    Topics: Adult; Body Dysmorphic Disorders; Citalopram; Comorbidity; Depressive Disorder; Double-Blind Method;

2016