Evidence map›Paper›PMID 28123299›Full record

ArticleNeuropsychiatric disease and treatment2017

Escitalopram versus paroxetine controlled release in major depressive disorder: a randomized trial.

Taro Kishi, Yuki Matsuda, Shinji Matsunaga, Masatsugu Moriwaki, Yoichiro Otake, Kaku Akamatsu, Tomo Okochi, Shigeki Hirano, Toshihiko Funahashi, Momoko Okuda and 3 more

Open access · goldAbstract read
In one paragraph

Article in Neuropsychiatric disease and treatment, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 37% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. 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

13 authors at 3 institutions in 1 country.

Taro KishiDepartment of Psychiatry, Fujita Health University School of Medicine.
Yuki MatsudaDepartment of Psychiatry, Fujita Health University School of Medicine.
Shinji MatsunagaDepartment of Psychiatry, Fujita Health University School of Medicine.
Masatsugu MoriwakiDepartment of Psychiatry, Fujita Health University School of Medicine; Department of Psychiatry, Okehazama Hospital, Toyoake.
Yoichiro OtakeDepartment of Psychiatry, Okehazama Hospital, Toyoake.
Kaku AkamatsuDepartment of Psychiatry, Jindai Clinic, Nagoya.
Tomo OkochiDepartment of Psychiatry, Toyota Memorial Hospital.
Shigeki HiranoDepartment of Psychiatry, Toyota Memorial Hospital.
Toshihiko FunahashiDepartment of Psychiatry, Jindai Hospital, Toyota, Aichi.
Momoko OkudaDepartment of Psychiatry, Holy Cross Hospital, Toki, Gifu, Japan.
Hideaki TabuseDepartment of Psychiatry, Holy Cross Hospital, Toki, Gifu, Japan.
Kiyoshi FujitaDepartment of Psychiatry, Okehazama Hospital, Toyoake.
Nakao IwataDepartment of Psychiatry, Fujita Health University School of Medicine.
Fujita Health University · JPGifu Red Cross Hospital · JPToyota Memorial Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThere are no direct comparisons between escitalopram and paroxetine controlled release in patients with major depressive disorder (MDD).

methodsWe conducted a 24-week, rater-masked, randomized trial of escitalopram (5-20 mg/day) versus paroxetine controlled release (12.5-50 mg/day) in patients with MDD (UMIN000011191). Patients with the diagnosis of moderate-to-severe MDD (a 17-item Hamilton Rating Scale for Depression [HAMD-17], with total score at baseline being ≥20) were recruited to participate in a parallel, randomized, controlled trial. The primary outcome for efficacy was an improvement in the 21-item HAMD (HAMD-21) total score at 24 weeks. The secondary outcomes were the response, remission, and discontinuation rates and the incidence of individual adverse events.

resultsA total of 88 patients with MDD (males, 61.4%; mean age, 40.8±13.4 years) were recruited. The discontinuation rate was 58.0% (escitalopram, 55.8%; paroxetine controlled release, 60.0%). Both escitalopram and paroxetine controlled-release treatment groups exhibited significant reduction in the HAMD-21 total score at 2, 4, 8, 12, and 24 weeks from the baseline. However, there were no significant differences in the HAMD-21 total score, response rate, remission rate, and discontinuation rate at any time point between the groups. In addition, there were no significant differences in the incidence of any individual adverse events (eg, nausea, vomiting, and somnolence) between the treatment groups.

conclusionOur results suggest that escitalopram and paroxetine controlled release had similar efficacy and safety profiles in patients with MDD. One of the primary limitations of this study is the small sample size.

Indexed as

antidepressantescitalopramHamilton Rating Scale for Depressionmajor depressive disorderparoxetine controlled release

Identifiers

PMID28123299
PMCPMC5230634
OpenAlexW2569566349

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.