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Clinical Trials/JPRN-UMIN000008422
JPRN-UMIN000008422Completed未知

Gastrointestinal Adverse effect with oral bisphophonate Survey - GAP Survey Research

Shimane University Faculty of Medicine0 sites200 target enrollmentStarted: July 17, 2012Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
200

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20years-old to 100years-old (—)
Sex
All

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1) Patient who has received bisphosphonates. However, after discontinuing these bisphosphonates for six months, it is possible to register. 2) Woman who are in pregnant or who hopes for pregnancy 3) Patient who has serious hepatopathy, renal damage, and cardiac disease 4) Patients judged as improper to participate for the clinical trial by physician in charge

Investigators

Sponsor
Shimane University Faculty of Medicine

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