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NCT01076426
The Clinical Use of Probiotics in the Uremia Patients Under Chronic Peritoneal Dialysis
Phase 4 trial testing Pro-biotics in Peritonitis in 100 participants. Status unknown.
1 March 2010
Quick facts
| Lead sponsor | National Cheng-Kung University Hospital |
|---|---|
| Phase | Phase 4 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | triple |
| Primary purpose | treatment |
| Enrollment | 100 |
| Start date | 1 February 2010 |
| Primary completion | 1 March 2010 |
| Estimated completion | 1 March 2011 |
| Sites | 1 location across Taiwan |
Drugs / interventions tested
- Pro-biotics — full drug profile →
- Oligosaccharide
Conditions studied
- Peritonitis — all drugs for Peritonitis →
- Malnutrition — all drugs for Malnutrition →
Sponsor
National Cheng-Kung University Hospital
Who can join
Adults 16 to 75, any sex, with Peritonitis or Malnutrition. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
peritonitis rate
Time frame: one year -
nutrition status
Time frame: 3, 6, 9, 12 months
Sponsor's own description
The purpose of this study is to determine whether probiotics can improve the nutrition status and prevent peritonitis in the chronic peritoneal dialysis patients.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT01076426
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Peritonitis
Currently open trials in the same condition.
- NCT04604730 — Role of Protective Stoma After Primary Anastomosis for Generalized Peritonitis Due to Perforated Diverticulitis · NA · recruiting
Other National Cheng-Kung University Hospital trials
Trials by the same sponsor.
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- NCT07257926 — Prevention of Delayed Post-polypectomy Bleeding by Endoscopic Sucralfate Spray in High-risk Patients: A Randomized Contr · Phase 4 · not yet recruiting
- NCT07269132 — Applying the ADDIE Model to Develop a Multimedia Program to Enhance Chemotherapy Knowledge and Self-Efficacy Among Inten · NA · enrolling by invitation
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 NCT01076426 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by National Cheng-Kung University Hospital
- Last refreshed: 25 February 2010
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/NCT01076426.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing