Evidence map›Paper›PMID 32993653›Full record

Trial reportBMC complementary medicine and therapies2020

Effectiveness of Echium amoenum on premenstrual syndrome: a randomized, double-blind, controlled trial.

Maryam Farahmand, Davood Khalili, Fahimeh Ramezani Tehrani, Gholamreza Amin, Reza Negarandeh

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC complementary medicine and therapies, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing 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.

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

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

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Management of Premenstrual Dysphoric Disorder: A Scoping Review.International journal of women's health · 2022
    Article
  7. Article
  8. Evaluation of the effect ofAvicenna journal of phytomedicine
    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

5 authors.

Maryam FarahmandNursing & Midwifery Care Research Center, School of Nursing and Midwifery, Tehran University of Medical Sciences, P.O.Box: 1419733171, Mirkhani St., Tohid Sq, Tehran, Iran.
Davood KhaliliPrevention of Metabolic Disorders Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Fahimeh Ramezani TehraniReproductive Endocrinology Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Gholamreza AminDepartment of Pharmacognosy, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Reza NegarandehNursing & Midwifery Care Research Center, School of Nursing and Midwifery, Tehran University of Medical Sciences, P.O.Box: 1419733171, Mirkhani St., Tohid Sq, Tehran, Iran. rnegarandeh@tums.ac.ir.ORCID http://orcid.org/0000-0002-7597-5094

Funding

Tehran University of Medical Sciences and Health Services 94-01-99-28715.
6 · The paper itself

Abstract

backgroundThe present study aimed to evaluate the effect of Echium amoenum (EA) on the severity of premenstrual syndrome (PMS) in comparison with placebo.

methodsThe present study was a randomized double-blind controlled clinical trial. A checklist questionnaire was completed by 120, 18 to 35-year-old, college students. And then, 84 eligible women (20 to 35 years old) were enrolled in the trial; they were randomly assigned to two groups of intervention (EA) and control (placebo), with 42 participants in each group. Participants in the intervention group received 450 mg capsules of EA per day (three times a day) from the 21st day of their menstrual cycle until the 3rd day of their next cycle for two consecutive cycles. The severity of PMS was measured and ranked using the premenstrual symptoms screening tool (PSST). The generalized estimating equation was used to compare the total score of the severity of PMS between the two groups.

resultsSixty-nine women with regular menstrual cycles suffering from PMS completed the study. The mean scores of the symptoms in the EA group were 35.3 and 16.1 (P ≤ 0.001) at baseline and after 2 months, respectively, while the mean scores of the symptoms in the placebo group were 31.0 and 28.3 (P = 0.09) at baseline and after 2 months, respectively. The evaluation of the first and the second follow-ups in the intervention group showed that, after being adjusted for age and body mass index (P ≤ 0.001), the mean scores of the premenstrual syndrome, using GEE analysis, have decreased to 6.2 and 11.6, respectively.

conclusionBased on the results, in comparison with the placebo group, EA was found to be more effective in improving the symptoms of PMS, and is highly recommended for treatment of this syndrome.

trial registrationIRCT2015110822779N3 ; Registration date: 2015-11-27.

Indexed as

EchiumAdultCapsulesDouble-Blind MethodFemaleHumansPhytotherapyPlant ExtractsPremenstrual SyndromeSurveys and QuestionnairesUniversitiesYoung AdultCapsulesPlant ExtractsEchium AmeonumHerbal medicinePhytosterolPremenstrual symptoms screening toolPremenstrual syndromeStarch

Identifiers

PMID32993653
PMCPMC7526142

What OpenQuestion holds

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LicenceCC BY
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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.