Evidence map›Paper›PMID 36599872›Full record

Trial reportScientific reports2023

A randomized trial of once daily versus twice daily dosing of oral iron in CKD.

Vivek Sood, Kajal Kamboj, Prateek Bhatia, Vishal Sharma, Monica Kundu, Arpita Ghosh, Sanjay Kumar Singh, Thakur Sen, Prabhjot Kaur, Raja Ramachandran and 7 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

17 authors at 2 institutions in 2 countries.

Vivek Sood *Department of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Kajal Kamboj *Department of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Prateek BhatiaDepartment of Paediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Vishal SharmaDepartment of Gastroenterology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Monica KunduGeorge Institute for Global Health, New Delhi, India.
Arpita GhoshGeorge Institute for Global Health, New Delhi, India.
Sanjay Kumar SinghDepartment of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Thakur SenDepartment of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Prabhjot KaurDepartment of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Raja RamachandranDepartment of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Manish RathiDepartment of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Harbir Singh KohliDepartment of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Krishan Lal GuptaDepartment of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Samir MalhotraDepartment of Pharmacology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Ashok Kumar YadavDepartment of Experimental Medicine and Biotechnology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Vivek KumarDepartment of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India. enigma165@yahoo.co.in.
Vivekanand JhaGeorge Institute for Global Health, New Delhi, India.
Post Graduate Institute of Medical Education and Research · INGeorge Institute for Global Health · IN

Funding

DBT-Wellcome Trust India Alliance IA/CPHI/18/1/503954
6 · The paper itself

Abstract

We investigated the effect of two dosing regimens of oral iron on iron status and hematological parameters in patients with CKD. In this single center, open label, randomized, active controlled clinical trial, stable adult patients with CKD stage G3-4 with percentage transferrin saturation (%TSAT) ≤ 30% and serum ferritin ≤ 500 ng/ml were eligible. Participants were randomized to receive either 100 mg of ferrous ascorbate once daily (OD group) or 100 mg of ferrous ascorbate twice daily (BD group, total daily dose 200 mg). The primary outcome was change in %TSAT between groups over 12 weeks. The secondary outcomes were changes in other iron status and hematological parameters, serum interleukin-6 (IL-6) and hepcidin. 80 participants were enrolled out of which 76 completed the study. Change in %TSAT was not significantly different between groups (β = - 1.43, 95% CI - 3.99 to 1.12, BD group as reference). The rise in serum ferritin was less in the OD group as compared to BD group (β = - 0.36, 95% CI - 0.61 to - 0.10) whereas MCHC increased in the OD group as compared to decrease in the BD group (β = 0.37, 95% CI 0.067-0.67). These observations need exploration to ascertain the impact of different oral iron dosing strategies in CKD.

Indexed as

Anemia, Iron-DeficiencyRenal Insufficiency, ChronicAdultAscorbic AcidFerritinsHumansIronAscorbic AcidFerritinsIron

Identifiers

PMID36599872
PMCPMC9813132
OpenAlexW4313544738

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.