Evidence map›Paper›PMID 24347282›Full record

Trial reportClinical drug investigation2014

Efficacy, safety, and tolerability of pantoprazole magnesium in the treatment of reflux symptoms in patients with gastroesophageal reflux disease (GERD): a prospective, multicenter, post-marketing observational study.

José María Remes-Troche, Sergio Sobrino-Cossío, Julio César Soto-Pérez, Oscar Teramoto-Matsubara, Miguel Morales-Arámbula, Antonio Orozco-Gamiz, José Luis Tamayo de la Cuesta, Gualberto Mateos

Abstract readClinical Trial, Phase IVMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Trial report in Clinical drug investigation, 2014. 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
0.2field-weighted citation impact, top 40% 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, 6 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
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 7 institutions in 1 country.

José María Remes-TrocheDigestive Physiology and Motility Lab, Instituto de Investigaciones Médico Biológicas, Universidad Veracruzana, Iturbide SN. Col Centro, Veracruz, VER, 91400, Mexico, jose.remes.troche@gmail.com.
Sergio Sobrino-Cossío
Julio César Soto-Pérez
Oscar Teramoto-Matsubara
Miguel Morales-Arámbula
Antonio Orozco-Gamiz
José Luis Tamayo de la Cuesta
Gualberto Mateos
Hospital Angeles Pedregal · MXHospital Civil de Guadalajara · MXInstituto Nacional de Cancerología · MXPediatric Hospital of Sinaloa · MXPemex (Mexico) · MXSecretaría de Salud de Jalisco · MXUniversidad Veracruzana · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo improve proton pump inhibitor effects, pharmacological modifications have been developed such as the use of enantiomer molecules (e.g., S-omeprazole, S-pantoprazole, or dexlansoprazole), or addition of NaHCO3 (for an immediate release) or magnesium (with a lower absorption for a more sustained effect).

objectiveThe objective of this study was to assess the efficacy, safety, and tolerability of pantoprazole magnesium 40 mg once daily for 4 weeks, on the relief of reflux symptoms in gastroesophageal reflux disease (GERD) patients.

methodsA phase IV, open-label, prospective, multicenter study was designed. Patients included were prescribed pantoprazole magnesium 40 mg orally once daily for 28±2 days. All patients had a history of persistent or recurrent heartburn and/or acid regurgitation for at least 3 months. Effectiveness and tolerability data obtained from patients who completed a minimum of 4 weeks of pantoprazole magnesium treatment were considered for analysis.

resultsThe account of baseline characteristics and demographics of GERD symptom intensity was made by analyzing the group of 4,343 patients that fulfilled all inclusion criteria; 54% were females (n=2,345) and 46% (n=1,998) males, with a mean age of 36.2±7.5 years. Severity of symptoms, assessed by the physician using the 4-point Likert scale, reduced by at least 80% from baseline intensity after treatment in the per protocol population. In the case of the intention-to-treat population, the improvement in symptom intensity was 73%. The number of patients that experienced any adverse events was 175/5,027 (3.48%).

conclusionsPantoprazole magnesium is a safe, effective, and well-tolerated drug that significantly improves GERD symptoms.

Indexed as

2-PyridinylmethylsulfinylbenzimidazolesAdultAnti-Ulcer AgentsFemaleGastroesophageal RefluxHeartburnHumansMalePantoprazoleProspective StudiesProton Pump InhibitorsSaltsTreatment Outcome2-PyridinylmethylsulfinylbenzimidazolesAnti-Ulcer AgentsPantoprazoleProton Pump InhibitorsSalts

Identifiers

PMID24347282
OpenAlexW2059976567

What OpenQuestion holds

Textmetadata
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.