ArticleBrain, behavior, & immunity - health2026
Celecoxib adjunct to antidepressants for major depressive disorder: Systematic review and meta-analysis.
Article in Brain, behavior, & immunity - health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This systematic review and meta-analysis of randomized, placebo-controlled trials evaluated the efficacy, acceptability, and tolerability of celecoxib as an adjunct to antidepressants for major depressive disorder (MDD). PubMed, Embase, the Cochrane Library, Google Scholar, and ClinicalTrials.gov were searched from inception to April 11, 2026. The primary outcome was change in depressive symptom severity. Secondary outcomes included all-cause dropouts and adverse-effect dropouts. The risk of bias in trials was assessed using the Cochrane Risk of Bias 2 tool. Standardized mean differences (SMDs) and risk ratios (RRs) were pooled using a random-effects model. Evidence certainty was rated using the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) approach. Seven trials were included (N = 365; 183 received celecoxib, 182 received placebo). Most trials administered celecoxib 400 mg/day for 6 weeks in patients without treatment-resistant depression. Adjunctive celecoxib significantly reduced depressive symptom severity compared with placebo (SMD = -0.63, 95% CI: -1.25 to -0.01;
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Registered trials
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