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<0,001); the reduction in abdominal pain was especially significant (p<0,001). The diary entries confirmed the reduction in abdominal pain and revealed a significant reduction in days with bloating (p<0,001). The Bristol-stool-scale analysis showed improvements; particularly, patients with IBS-D benefited from the treatment (p<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 |