Evidence map›Paper›PMID 38454079›Full record

Trial reportMolecular psychiatry2024

Comparative effectiveness research trial for antidepressant incomplete and non-responders with treatment resistant depression (ASCERTAIN-TRD) a randomized clinical trial.

George I Papakostas, Madhukar H Trivedi, Richard C Shelton, Dan V Iosifescu, Michael E Thase, Manish K Jha, Sanjay J Mathew, Charles DeBattista, Mehmet E Dokucu, Olga Brawman-Mintzer and 12 more

Registry-linked trialAbstract readRandomized Controlled TrialMulticenter StudyComparative Study
In one paragraph

Trial report in Molecular psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02977299 (Augmentation Versus Switch), which is not on this map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02977299 phase4completednot on this map

Augmentation Versus Switch: Comparative Effectiveness Research Trial for Antidepressant Incomplete and Non-responders With Treatment Resistant Depression (ASCERTAIN-TRD)

TypeinterventionalSponsorMassachusetts General HospitalRan2017 to 2022Enrolled278ConditionsTreatment Resistant Major Depressive DisorderArmsAripiprazole, Repetitive transcranial magnetic stimulation (rTMS), Venlafaxine XR
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Review
  7. Article
  8. Review
  9. Revisiting the Management of Treatment-Resistant Depression.Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2026
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Advances in the Clinical Application of Neurostimulation in Major Depression.Advances in experimental medicine and biology · 2026
    Review
  16. Article
  17. Article
  18. Open letter to the Medical Services Advisory Committee regarding TMS Item Number regulations.Australasian psychiatry : bulletin of Royal Australian and New Zealand College of Psychiatrists · 2025
    Article
  19. Genetics of Response to ECT, TMS, Ketamine and Esketamine.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2025
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

George I PapakostasMassachusetts General Hospital and Harvard Medical School, Boston, MA, USA. gpapakostas@mgb.org.
Madhukar H TrivediUniversity of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-2983-1110
Richard C SheltonUniversity of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0000-0002-3806-4208
Dan V IosifescuNathan Kline Institute for Psychiatric Research and New York University School of Medicine, New York, NY, USA.
Michael E ThasePerelman School of Medicine of the University of Pennsylvania, Philadelphia, PA, USA.
Manish K JhaUniversity of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-2764-2391
Sanjay J MathewBaylor College of Medicine, Houston, TX, USA.ORCID 0000-0002-2715-6641
Charles DeBattistaStanford University School of Medicine, Stanford, CA, USA.
Mehmet E DokucuDartmouth Geisel School of Medicine, Lebanon, NH, USA.
Olga Brawman-MintzerMedical University of South Carolina, Charleston, SC, USA.
Glenn W CurrierMorsani College of Medicine, University of South Florida, Tampa, FL, USA.
William Vaughn McCallMedical College of Georgia, Augusta, GA, USA.ORCID 0000-0001-5035-7858
Mandana ModirroustaUniversity of Manitoba, Winnipeg, MB, Canada.
Matthew MacalusoUniversity of Alabama at Birmingham, Birmingham, AL, USA.
Alexander BystritskySemel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, LA, USA.
Fidel Vila RodriguezUniversity of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-8273-8820
Erik B NelsonUniversity of Cincinnati Academic Health Center, Cincinnati, OH, USA.
Albert S YeungMassachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Anna FeeneyMassachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Leslie C MacGregorMassachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Thomas CarmodyUniversity of Texas Southwestern Medical Center, Dallas, TX, USA.
Maurizio FavaMassachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Funding

Patient-Centered Outcomes Research Institute (PCORI) TRD-1511-33227
6 · The paper itself

Abstract

Further research is needed to help improve both the standard of care and the outcome for patients with treatment-resistant depression. A particularly critical evidence gap exists with respect to whether pharmacological or non-pharmacological augmentation is superior to antidepressant switch, or vice-versa. The objective of this study was to compare the effectiveness of augmentation with aripiprazole or repetitive transcranial magnetic stimulation versus switching to the antidepressant venlafaxine XR (or duloxetine for those not eligible to receive venlafaxine) for treatment-resistant depression. In this multi-site, 8-week, randomized, open-label study, 278 subjects (196 females and 82 males, mean age 45.6 years (SD 15.3)) with treatment-resistant depression were assigned in a 1:1:1 fashion to treatment with either of these three interventions; 235 subjects completed the study. 260 randomized subjects with at least one post-baseline Montgomery-Asberg Depression Rating (MADRS) assessment were included in the analysis. Repetitive transcranial magnetic stimulation (score change (standard error (se)) = -17.39 (1.3) (p = 0.015) but not aripiprazole augmentation (score change (se) = -14.9 (1.1) (p = 0.069) was superior to switch (score change (se) = -13.22 (1.1)) on the MADRS. Aripiprazole (mean change (se) = -37.79 (2.9) (p = 0.003) but not repetitive transcranial magnetic stimulation augmentation (mean change (se) = -42.96 (3.6) (p = 0.031) was superior to switch (mean change (se) = -34.45 (3.0)) on the symptoms of depression questionnaire. Repetitive transcranial magnetic stimulation augmentation was shown to be more effective than switching antidepressants in treatment-resistant depression on the study primary measure. In light of these findings, clinicians should consider repetitive transcranial magnetic stimulation augmentation early-on for treatment-resistant depression.Trial registration: ClinicalTrials.gov, NCT02977299.

Indexed as

Antidepressive AgentsAripiprazoleDepressive Disorder, Treatment-ResistantTranscranial Magnetic StimulationVenlafaxine HydrochlorideAdultCombined Modality TherapyComparative Effectiveness ResearchDuloxetine HydrochlorideFemaleHumansMaleMiddle AgedPsychiatric Status Rating ScalesTreatment OutcomeAntidepressive AgentsAripiprazoleDuloxetine HydrochlorideVenlafaxine Hydrochloride

Identifiers

PMID38454079
PMCPMC11412904

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.