An Observational Study Measuring Outcomes in Cancer Patients Treated for Moderate to Severe Hyponatremia in Italy

NCT ID: NCT02573077

Last Updated: 2018-04-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

69 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-10-31

Study Completion Date

2017-12-13

Brief Summary

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This observational, prospective, non-interventional study will include cancer patients who need a treatment for hyponatraemia secondary to SIADH. Patients will be prescribed treatment(s) according with the clinical practice regardless of the patient participation in the study. The purpose of this NIS is to collect additional scientific and clinical information that can help in describing the characteristics of cancer patients with hyponatraemia secondary to SIADH, the current management of hyponatremia, the therapies to keep under control serum \[Na+\] and the guidelines for the management of this population in Italy.

Detailed Description

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Conditions

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Hyponatremia Syndrome of Inappropriate ADH (SIADH) Secretion Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

1. Age \>= 18 years;
2. Male or female patients with a cytologically or histologically documented cancer diagnosis;
3. Moderate to severe hyponatremia: Na+ level cut off: \[Na+\] \< 130 mmol/L;
4. Physician diagnosed Moderate to severe hyponatremia secondary to SIADH (clinical or laboratory determined as per normal routine practice of treating physician);
5. No use of diuretic agents within the week prior to evaluation;
6. Willingness to participate in the study; subjects must give their written consent to participate.

Exclusion Criteria

1. Use of concomitant medications including demeclocycline and/or urea, by themselves or in combination with fluid restriction;
2. Subject is currently participating in a clinical trial in which the investigational medicinal product aims to treat the causes or symptoms of hyponatremia;
3. Life expectancy is lower than 3 months.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Otsuka Pharmaceutical Europe Ltd

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Medical Department

Role: STUDY_DIRECTOR

Otsuka Europe

Locations

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Ancona, , Italy

Site Status

Aosta, , Italy

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Bari, , Italy

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Cagliari, , Italy

Site Status

Cosenza, , Italy

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Florence, , Italy

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Genova, , Italy

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Messina, , Italy

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Milan, , Italy

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Napoli, , Italy

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Negrar, , Italy

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Novara, , Italy

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Palermo, , Italy

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Parma, , Italy

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Perugia, , Italy

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Piacenza, , Italy

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Pisa, , Italy

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Roma, , Italy

Site Status

Varese, , Italy

Site Status

Verona, , Italy

Site Status

Countries

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Italy

Other Identifiers

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OPEL/2014/067

Identifier Type: -

Identifier Source: org_study_id

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