Evidence map›Paper›PMID 34195029›Full record

ArticleJournal of traditional and complementary medicine2021

Phase I clinical trial to evaluate the safety and pharmacokinetics of capsule formulation of the standardized extract of

Kesara Na-Bangchang, Inthuorn Kulma, Tullayakorn Plengsuriyakarn, Thipaporn Tharavanij, Kanawut Kotawng, Anurak Chemung, Nadda Muhamad, Juntra Karbwang

Open access · diamondAbstract read
In one paragraph

Article in Journal of traditional and complementary medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
7.1field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
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  18. Bioassay for total serum bioactivity ofJournal of advanced pharmaceutical technology & research
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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 1 institution in 1 country.

Kesara Na-BangchangGraduate Studies, Chulabhorn International College of Medicine, Thammasat University, Pathumthani, 12120, Thailand.
Inthuorn KulmaGraduate Studies, Chulabhorn International College of Medicine, Thammasat University, Pathumthani, 12120, Thailand.
Tullayakorn PlengsuriyakarnGraduate Studies, Chulabhorn International College of Medicine, Thammasat University, Pathumthani, 12120, Thailand.
Thipaporn TharavanijFaculty of Medicine, Thammasat University, Pathumthani, 12120, Thailand.
Kanawut KotawngGraduate Studies, Chulabhorn International College of Medicine, Thammasat University, Pathumthani, 12120, Thailand.
Anurak ChemungGraduate Studies, Chulabhorn International College of Medicine, Thammasat University, Pathumthani, 12120, Thailand.
Nadda MuhamadGraduate Studies, Chulabhorn International College of Medicine, Thammasat University, Pathumthani, 12120, Thailand.
Juntra KarbwangCenter of Excellence in Pharmacology and Molecular Biology of Malaria and Cholangiocarcinoma, Thammasat University, Pathumthani, 12120, Thailand.
Thammasat University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimEXPERIMENTAL PROCEDURE: Forty-eight healthy Thai participants who fulfilled the inclusion and had none of the exclusion criteria were allocated to two study groups. The RESULTS AND

conclusionThe AL extract was well tolerated in both groups. Atractylodin was rapidly absorbed but with low systemic exposure and residence time. There was no difference in the pharmacokinetic parameters of atractylodin following a single or multiple dosing, suggesting the absence of accumulation and dose-dependency in human plasma after continuous dosing for 21 days. The information on human pharmacokinetics of AL, when given as capsule formulation of the standardized extract, would assist in further dose optimization in cholangiocarcinoma patients with the defined pharmacokinetic-pharmacodynamic relationship.

Indexed as

Atractylodes lanceaAtractylodinPharmacokineticsPhase I clinical trialSafety

Identifiers

PMID34195029
PMCPMC8240349
OpenAlexW3128042207

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.