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Clinical Trials/NCT05442177
NCT05442177
Completed
Not Applicable

Clinical Observation of Integrated Chinese Medicine With Western Medicine for the Reduction of Chemotherapy-induced Hematologic Toxicity

Taichung Tzu Chi Hospital0 sites35 target enrollmentJuly 1, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myelosuppression
Sponsor
Taichung Tzu Chi Hospital
Enrollment
35
Primary Endpoint
Chemotherapy-induced Hematologic Toxicity
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

We conducted an observational study to investigate the effectiveness and safety of Integrated Chinese Medicine With Western Medicine for bone marrow suppression induced by chemotherapy in patients with cancer. The TCM constitution and pulse diagnosis was also observed in the study.

Detailed Description

Patients with cancer under chemotherapy and integrated Western and Chinese medicine were enrolled in this observational study. The assessment of radial pressure pulse (RPP) was performed before and after chemotherapy. The correlation between the spectral energy (SE0-10 Hz, SE10-50 Hz, and SE13-50 Hz) of the RPP at six diagnosis positions and the blood cell counts before and after chemotherapy were analyzed.

Registry
clinicaltrials.gov
Start Date
July 1, 2015
End Date
June 30, 2016
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Taichung Tzu Chi Hospital
Responsible Party
Principal Investigator
Principal Investigator

Chia-Ying Chuang

Chinese medicine department

Taichung Tzu Chi Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients with cancer diagnosed through pathological histology
  • Patients with cancer under chemotherapy and Integrated Chinese Medicine With Western Medicine
  • Patients with an Eastern Cooperative Oncology Group Performance score of 0-2
  • Patients having normal liver and kidney functions and electrocardiography and eligible for chemotherapy with normal bone marrow hematopoietic function
  • Patients who were voluntarily involved in this study

Exclusion Criteria

  • Cases that did not meet the inclusion criteria
  • Patients who could not cooperate with pulse diagnosis
  • Patients with underlying diseases such as chronic obstructive pulmonary disease, cardiac failure, chronic renal failure, cirrhosis, etc.
  • Patients with severe infection
  • Patients with severe cachexia

Outcomes

Primary Outcomes

Chemotherapy-induced Hematologic Toxicity

Time Frame: one month

the blood cell count before and after chemotherapy was collected for measurement of severity of myelosuppression

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