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Comparision of bixalomer (Kiklin) dose timing as phosphate binder and impact in HD patients

Comparision of bixalomer (Kiklin) dose timing as phosphate binder and impact in HD patients - Skip-study 2

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009792
Enrollment
30
Registered
2013-04-01
Start date
2013-04-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemodialysis patients with hyperphosphatemia

Interventions

1) Bixalomer: The patients managed hyperphosphatemia with taking bixalomer just before each meal will take them after each meal. The dose of bixalomer is fixed during the observation. The level of

Sponsors

Juntendo University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients are eligible if they are compatible with the following criteria. 1.hemodialysis patients complicated with hyperphosphorous who managed with bixalomer. 2.30 patients with agreement for exchange of midication mode from taking bixalomer before meal to after meal. 3.Patients who is available for the record to questionnaires (an abdominal symptom, medication situation questionnaire). 4.Patients who we agreed with the participation of the study based on informed consent before the study initiation, and filled in signature sealing or a signature and a date

Exclusion criteria

Exclusion criteria: ients are excluded if they are compatible with any one of the following criteria. 1.Patients with a history of hypersensitivity for an ingredient of this medicine 2.Patients with bowel obstruction (for a non-absorbable polymer, we might raise intestinal perforation) 3.Patients with significant psychic disturbance or drug dependence disease or alcoholism 4.Patients that going to hospital of all follow-up seems to be impossible 5.Patients who are not able to understand a test instructions from medical experts of the client side or the doctors involved in the study 6.Patients who judged as inadequate by the doctors involved in the study

Design outcomes

Primary

MeasureTime frame
Level of serum phosphate

Secondary

MeasureTime frame
Evaluation of efficacy *Blood gas concentrations *Abdominal symptoms evaluation *Drug remedy time estimation *Adverse events

Countries

Japan

Contacts

Public ContactChieko Hamada

Juntendo University Faculty of Medicine Department of Internal Medicine, Division of Nephrology

chieko@juntendo.ac.jp03-3813-1183

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026