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Clinical Trials/JPRN-UMIN000006016
JPRN-UMIN000006016
Not yet recruiting
未知

Phase 2 study of combination chemotherapy(VBL/PSL, MTX, 6MP) in patients with primary untreated adult langerhans cell histiocytosis - Combination chemotherapy in patients with primary untreated adult langerhans cell histiocytosis

Department of Hematology, International Medical Center, Saitama Medical University0 sites5 target enrollmentAugust 1, 2011

Overview

Phase
未知
Intervention
Not specified
Conditions
adult langerhans cell histiocytosis
Sponsor
Department of Hematology, International Medical Center, Saitama Medical University
Enrollment
5
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 1, 2011
End Date
March 31, 2020
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Department of Hematology, International Medical Center, Saitama Medical University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • A patient is uneligible if he (she) has (a) to (m). (a) SaO2 bellow 93% in room air. (b) Serum Cr level above 2\.0 mg/dL. (c) T.Bil level above 2\.0 mg/dL or GPT over 4 times of upper limit. (d) Uncontrolable DM using insurin. (e) Uncontrolable Hypertention. (f) History of myocardial infarction, congestive heart failure, unstable angina. (g) Resting ejection fraction bellow 50% by UCG. (h) Have an active cancer. (i) On or taking major tranquilizer, antidepressant, antimanic. (j) Uncontrollable active infection. (k) History of adverse reaction for the agents included in the protocol (l) Woman who is pregnant, possibly pregnant or breast feeding. (m) Inadequate for clinical trial entry by the attending physicians.

Outcomes

Primary Outcomes

Not specified

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