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Trial · NCT02083926

Ketamine Infusion for Social Anxiety Disorder

NCT02083926, Early phase 1, Completed, Yale University; results first posted 2021-03-18

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Ketamine Infusion for Social Anxiety Disorder. Trials, record NCT02083926. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02083926

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Ketamine Infusion for Social Anxiety Disorder
NCT number
NCT02083926
Status
Completed
Phases
Early phase 1
Enrollment
18 participants, actual
Lead sponsor
Yale University
Conditions
Social Anxiety Disorder
Interventions
Ketamine, Saline
First posted
2014-03-11
Last updated
2021-03-18
Results first posted
2021-03-18
Limitations and caveats
A significant limitation of our study was that 17 of 18 subjects correctly identified when they received ketamine, suggesting that the use of saline as a placebo control for ketamine led to inadequate blinding.

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryVisual Analogue Scale for Anxiety Symptoms (VAS-anxiety)Day 1 (1+28)
Instrument that tries to measure anxiety, that is believed to range across a continuum of values and cannot easily be directly measured.We used a straight horizontal line of 100 mm in length. The ends were defined as the extreme limits of the parameter to be measured (anxiety); oriented from the left (no anxiety) to the right (worst anxiety ever felt). The patient marks on the line the point that they feel represents their perception of their current state.The VAS score is determined by measuring in millimeters from the left hand end of the line to the point that the patient marks. We examined Visual Analog Scale (VAS) for anxiety symptoms at screening, 1 hour prior to infusion, 1, 2 and 3 hours after infusion, 1, 2, 3, 5, 7, 10, and 14 days following a single ketamine/saline infusion.
PrimaryLiebowitz Social Anxiety Score (LSAS)Day 1 (1+28)
Clinician-administered scale for the assessment of fear and avoidance found in social phobia (SAD); it has 24 items divided into 2 subscales, 13 for performance anxiety, and 11 for social situations each rated from 0 to 3 (0=none,1=mild,2=moderate,3=definite). The sum scores for Fear and Avoidance results in an overall score (max 144 points). There are 4 clinician subscales: fear of social interaction, fear of performance, avoidance of social interaction and avoidance of performance 0 to 30= SAD is unlikely 30 to 60=SAD is probable 60 to 90=SADis very probable \>90= SAD highly probable

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYVisual Analogue Scale for Anxiety Symptoms (VAS-anxiety)Day 1 (1+28)units on a scaleMEAN
PRIMARYLiebowitz Social Anxiety Score (LSAS)Day 1 (1+28)score on a scaleMEAN

Results by group4

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Visual Analogue Scale for Anxiety Symptoms (VAS-anxiety)Ketamine Infusion on Day 0 or Day 2812.1Standard Deviation 18.6units on a scale
Visual Analogue Scale for Anxiety Symptoms (VAS-anxiety)Saline Infusion on Day 0 or Day 2819.6Standard Deviation 18.5units on a scale
Liebowitz Social Anxiety Score (LSAS)Ketamine Infusion on Day 0 or Day 2866.1Standard Deviation 30.9score on a scale
Liebowitz Social Anxiety Score (LSAS)Saline Infusion on Day 0 or Day 2886.1Standard Deviation 30score on a scale

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDKetamine Infusion on Day 0, Saline Infusion on Day 289
Overall StudySTARTEDSaline Infusion on Day 0, Ketamine Infusion on Day 289
Overall StudyCOMPLETEDKetamine Infusion on Day 0, Saline Infusion on Day 288
Overall StudyCOMPLETEDSaline Infusion on Day 0, Ketamine Infusion on Day 289
Overall StudyNOT COMPLETEDKetamine Infusion on Day 0, Saline Infusion on Day 281
Overall StudyNOT COMPLETEDSaline Infusion on Day 0, Ketamine Infusion on Day 280

Adverse events54

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherthings seem to be movingNervous system disordersKetamine Infusion on Day 0 or Day 287187
otherthings seem to be movingNervous system disordersSaline Infusion on Day 0 or Day 282172
otherthings seem unrealNervous system disordersKetamine Infusion on Day 0 or Day 289189
otherthings seem unrealNervous system disordersSaline Infusion on Day 0 or Day 283173
otherfeel like you are separated from realityNervous system disordersKetamine Infusion on Day 0 or Day 283183
otherfeel like you are separated from realityNervous system disordersSaline Infusion on Day 0 or Day 281171
otherlooking at things outside of your bodyNervous system disordersKetamine Infusion on Day 0 or Day 284184
otherlooking at things outside of your bodyNervous system disordersSaline Infusion on Day 0 or Day 280170
otherFeel like a spectatorNervous system disordersKetamine Infusion on Day 0 or Day 287187
otherFeel like a spectatorNervous system disordersSaline Infusion on Day 0 or Day 282172

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityKetamine Infusion on Day 0 or Day 28018
Total, all-cause mortalitySaline Infusion on Day 0 or Day 28017
Total, other adverse eventsKetamine Infusion on Day 0 or Day 281518
Total, other adverse eventsSaline Infusion on Day 0 or Day 28417
Total, serious adverse eventsKetamine Infusion on Day 0 or Day 28018
Total, serious adverse eventsSaline Infusion on Day 0 or Day 28017

Papers6

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
4899510BACKGROUNDPubMed
17346609BACKGROUNDPubMed
20206659BACKGROUNDPubMed
27604566BACKGROUNDPubMed
28441895BACKGROUNDPubMed
28849779DERIVEDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons2

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
Ketamine Infusion on Day 0 or Day 28 vs Saline Infusion on Day 0 or Day 28: deaths from any causeTrial comparisons
Ketamine Infusion on Day 0 or Day 28 vs Saline Infusion on Day 0 or Day 28: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02083926

GET https://conductscience.org/api/trials/v1/NCT02083926/events?page=2