PMA – Zeolite (Clinoptilolite) in the Management of Irritable Bowel Syndrome – a Non-Interventional Study

dc.contributor.author Mosgoeller, Wilhelm
dc.contributor.author Muss, Claus
dc.contributor.author Eisenwagen, Sandra
dc.contributor.author Jagsch, Reinhold
dc.contributor.author Vogelsang, Harald
dc.date.accessioned 2025-06-17T13:36:58Z
dc.date.available 2025-06-17T13:36:58Z
dc.date.issued 2024-01-15
dc.description.abstract <jats:title>Abstract</jats:title><jats:p>In clinical practice, the treatment of patients with irritable bowel syndrome (IBS) can be very challenging. The aims of the present non-interventional study (NIS) were to investigate the tolerability and efficacy of PMA-zeolite under everyday conditions in patients with diarrheic IBS type (IBS-D) or constipated type (IBS-C) or mixed type (IBS-M).</jats:p><jats:p> Methods To document prospective data on tolerability and symptom frequency in the frame of a nationwide NIS, we recruited 204 IBS patients. The study focused on the IBS-related quality of life (measured by the SF-36 questionnaire) and improvements of IBS-related symptoms according to specific ROM-III criteria and stool consistency (Bristol stool scale). The participants documented their abdominal pain, bloating, number of bowel movements, and stool consistency through a web-based internet platform (initial and exit questionnaires) and daily diary entries over the period of intake (8 weeks).</jats:p><jats:p> Results A total of 82.2% of the recruited patients had filled in the questionnaires before and after the 8-week treatment with PMA-zeolite. Seven of the eight subscales of the SF-36 improved significantly (p&lt;0,001); the reduction in abdominal pain was especially significant (p&lt;0,001). The diary entries confirmed the reduction in abdominal pain and revealed a significant reduction in days with bloating (p&lt;0,001). The Bristol-stool-scale analysis showed improvements; particularly, patients with IBS-D benefited from the treatment (p&lt;0,001). </jats:p><jats:p> Conclusion The treatment duration of 8 weeks was well tolerated by most patients. Under everyday life conditions, PMA-zeolite alleviated the global IBS-related symptoms and raised the quality of life (QOL). The PMA-zeolite, thus, may represent a good adjuvant therapeutic option for patients with irritable bowel syndrome.</jats:p>
dc.description.epage 387
dc.description.spage 379
dc.description.volume 62
dc.identifier.doi 10.1055/a-2223-3963
dc.identifier.issn 0044-2771
dc.identifier.issn 1439-7803
dc.identifier.openaire doi_dedup___:7a9d54a67b1ab1a42946bd9ec3a6f34f
dc.identifier.pmid 38224685
dc.identifier.uri https://ror.circle-u.eu/handle/123456789/754215
dc.openaire.affiliation University of Vienna
dc.openaire.collaboration 1
dc.publisher Georg Thieme Verlag KG
dc.rights OPEN
dc.rights.license CC BY NC ND
dc.source Zeitschrift für Gastroenterologie
dc.subject irritable bowel syndrome
dc.subject PMA-zeolite as adjuvant remedy
dc.subject 501010 Klinische Psychologie
dc.subject IBS
dc.subject 302016 Gastroenterologie
dc.subject observational (non-interventional) study
dc.subject 501010 Clinical psychology
dc.subject 302016 Gastroenterology
dc.title PMA – Zeolite (Clinoptilolite) in the Management of Irritable Bowel Syndrome – a Non-Interventional Study
dc.type publication

Files

Collections