Evidence map›Paper›PMID 35221703›Full record

ArticleClinical, cosmetic and investigational dermatology2022

A Comparative, Three-Arm, Randomized Clinical Trial to Evaluate the Effectiveness and Tolerability of Bilastine vs Fexofenadine vs Levocetirizine at the Standard Dose and Bilastine vs Fexofenadine at Higher Than the Standard Dose (Up-Dosing) vs Levocetirizine and Hydroxyzine (in Combination) in Patients with Chronic Spontaneous Urticaria.

Bela Shah, Dhiraj Dhoot, Ankita Choudhary, Neha Jangid, Deval Mistry, Shikha Shah, Shruti Kamat, Hanmant Barkate

Open access · goldAbstract read
In one paragraph

Article in Clinical, cosmetic and investigational dermatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

12 citing papers in PubMed, 1 citations in OpenAlex.

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  8. Advances in clinical application of HZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
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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

8 authors at 2 institutions in 1 country.

Bela ShahDepartment of Dermatology, Venereology and Leprosy, B.J.Medical College, Civil Hospital, Ahmedabad, India.
Dhiraj DhootDGM, Department of Global Medical Affairs, Glenmark Pharmaceuticals Ltd, Mumbai, India.ORCID 0000-0002-2045-9324
Ankita ChoudharyDepartment of Dermatology, Venereology and Leprosy, B.J.Medical College, Civil Hospital, Ahmedabad, India.
Neha JangidDepartment of Dermatology, Venereology and Leprosy, B.J.Medical College, Civil Hospital, Ahmedabad, India.
Deval MistryDepartment of Dermatology, Venereology and Leprosy, B.J.Medical College, Civil Hospital, Ahmedabad, India.
Shikha ShahDepartment of Dermatology, Venereology and Leprosy, B.J.Medical College, Civil Hospital, Ahmedabad, India.
Shruti KamatDepartment of Dermatology, Venereology and Leprosy, B.J.Medical College, Civil Hospital, Ahmedabad, India.
Hanmant BarkateDepartment of Global Medical Affairs, Glenmark Pharmaceuticals Ltd, Mumbai, India.
B.J. Medical College · INGlenmark Pharmaceuticals (India) · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThough second-generation antihistamines (SGAH) are first-line drugs in chronic spontaneous urticaria (CSU), 50% of patients do not respond to them. In such patients, guidelines recommend either up-dosing of SGAH or combination of different antihistamines. However, the studies comparing these treatment regimens are limited.

methodsIn this comparative, three-arm study, CSU patients were randomized to receive standard dose of either bilastine, fexofenadine, or levocetirizine for 2 weeks. After 2 weeks of treatment, non-responders received double dose of either bilastine or fexofenadine, while hydroxyzine 25 mg once daily was added in the levocetirizine group. Patients were primarily evaluated for improvement in CSU, quality of life, and somnolence.

resultsA total of 110 patients with CSU were recruited. At the end of 4 weeks, 33/39, 26/35, and 22/36 patients in the bilastine, fexofenadine, and levocetirizine groups showed improvement in urticaria symptoms. At week 2, there was no statistical difference in urticaria activity score (UAS7) improvement between any of the groups; however, at week 4, there was a statistical difference between the bilastine and levocetirizine groups (

conclusionTwo-fold up-dosing of bilastine improves CSU symptoms without compromising safety as compared to two-fold up-dosing of fexofenadine and combination of first- and second-generation antihistamines.

Indexed as

bilastinechronic spontaneous urticariafexofenadinehydroxyzinelevocetirizineup dosing

Identifiers

PMID35221703
PMCPMC8867222
OpenAlexW4213350912

What OpenQuestion holds

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LicenceCC BY-NC
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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.