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NCT06724198
Bowel Dysfunction After Low Rectal Resection. An Pilot Study Using Psyllium Husk In Rectal Cancer Patients.
NA trial testing Psyllium husk in Low Anterior Resection Syndrome in 20 participants. Participants enrolled and being followed up; not accepting new ones.
1 July 2025
Quick facts
| Lead sponsor | Sykehuset Telemark |
|---|---|
| Phase | NA |
| Status | Active, enrolled |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 20 |
| Start date | 1 January 2025 |
| Primary completion | 1 July 2025 |
| Estimated completion | 1 September 2025 |
| Sites | 1 location across Norway |
Drugs / interventions tested
- Psyllium husk — full drug profile →
Conditions studied
- Low Anterior Resection Syndrome — all drugs for Low Anterior Resection Syndrome →
- Quality of Life (QOL) — all drugs for Quality of Life (QOL) →
Sponsor
Sykehuset Telemark — full company profile →
Who can join
18 and older, any sex, with Low Anterior Resection Syndrome or Quality of Life (QOL). Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Rectal cancer constitutes 1/3 of more than 4500 annually diagnosed cases of colorectal (CRC) in Norway. With the advances in radiochemotherapy, and surgical techniques, the long-term survival rate is increasing after surgery regardless of the rising incidences, with a 73% 5-year survival rate in Norway (89% for stage I-III cancer). Low anterior resection (LAR) is the most commonly performed surgical procedure with curative intent with over 500 procedures per year in Norway alone. 80 % of patients subjected to LAR suffer from the LAR syndrome (LARS) which includes grades of bowel incontinence, urgency and tenesmus contributing to reduced quality of life (QoL). Suggested means of management have been advocated without preceding randomized trials. Psyllium husk has been suggested as a nutritional supplement for symptom reduction in patients suffering from LARS, but data is limited and no larger, randomized studies regarding its effect on patients with low anterior resection syndrome have been conducted. In this pilot study preceeding a placebo-controlled RCT, the investigators aim to improve documentation of a proposed management strategy. The investigators anticipate that a reduction in intestinal symptomburden will increase QoL for this large patientgroup.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Effect of psyllium husk on low anterior resection syndrome after rectal cancer surgery-a pilot prospective cohort study.
Holte SS, Avaliani N, Hoff G, Kazaryan AM, et al · · 2025 · PMID 41446326 · DOI 10.3389/fsurg.2025.1686486
Verify or expand the search:
- PubMed search for NCT06724198
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Low Anterior Resection Syndrome
Currently open trials in the same condition.
- NCT07537998 — Antegrade Intestinal Fluid Reinfusion for Prevention of Low Anterior Resection Syndrome After Low Anterior Resection: a · Phase 2, PHASE3 · recruiting
- NCT06424522 — A Bowel Management Program (Retrograde Rectal Enema) for the Treatment of Low Anterior Resection Syndrome in Rectal Canc · NA · recruiting
- NCT06758830 — Total Neoadjuvant Therapy and Organ Preservation Versus Surgery for Rectal Cancer. · Phase 2, PHASE3 · recruiting
- NCT06222255 — The Safety and Efficacy of Transanal Irrigation in Patients With Sleep Disturbance From Low Anterior Resection Syndrome · NA · recruiting
- NCT05943444 — Comparison of Postoperative Anal Function Between Parks and Bacon Techniques in Low Rectal Cancer · NA · recruiting
Other Sykehuset Telemark trials
Trials by the same sponsor.
- NCT05227729 — Descending Aorta Blood Flow to Guide Fluid Therapy During Surgery · completed
- NCT04763720 — Implementing Dyadic Developmental Psychotherapy (DDP) - Evaluation Research · enrolling by invitation
- NCT05138055 — The NOrwegian Tick-borne Encephalitis Study · active not recruiting
- NCT04514003 — The Corona and COVID-19 Study in Telemark and Agder · active not recruiting
- NCT04219020 — Pain Burden in Children and Adolescents With Cerebral Palsy · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06724198 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sykehuset Telemark
- Last refreshed: 9 July 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06724198.
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