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iving/ deceased donor intestinal transplantation using standardized immunosuppression protocol

Not Applicable
Conditions
irreversible intestinal failure
Registration Number
JPRN-UMIN000030454
Lead Sponsor
Tohoku University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
5
Inclusion Criteria

Not provided

Exclusion Criteria

Patients having allergy to immunosuppressive drug Pregnant or breast feeding female patients Patients having uncontrollable infection Patients having uncontrollable malignancy Patients having uncontrollable mental disorders

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patient and graft survival after intestinal transplantation rejection rate after transplantation
Secondary Outcome Measures
NameTimeMethod
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