Current Survey on Chemotherapy-Related Myelosuppression and Clinical Management in Chinese County-level Tumor Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorThe First Affiliated Hospital of Xinxiang Medical College

About this trial

Current Survey on Chemotherapy-Related Myelosuppression and Clinical Management in Chinese County-level Tumor Patients

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

The confirmed malignant tumor is one of the non-small cell lung cancer/small cell lung cancer/breast cancer/gastric cancer/esophageal cancer/colorectal cancer/gynecological malignant tumor (ovarian cancer, cervical cancer, endometrial cancer).

Patients who need to receive chemotherapy in the past 3 months and should continue to receive chemotherapy in the future

The relevant diagnosis and treatment information involved in the survey is complete: only patients with at least 1-2 examination results after 1 week after chemotherapy can be included

Understand and sign the informed consent form

Disqualifiers

Patients with concurrent chemoradiotherapy,

Patients with sequential chemoradiotherapy, and the irradiation site of radiotherapy is flat bone, sternum, and pelvis;

Patients with active bleeding before or during treatment; If the patient has received targeted drugs such as CDK4/6 inhibitors or chidaaniline in the front-line treatment, which have a great impact on the blood phase, the drug can be discontinued for at least half a month before it can be included

Patients who, in the opinion of other physicians, would cause non-chemotherapy-related myelosuppression

Trial population

Chinese County-level Tumor Patients

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • No intervention; Observational study

    Other intervention

    No intervention

Treatment groups

1,000 Participants
are divided into 3 treatment groups
Group A: Chemotherapy-Related Myelosuppression1 intervention
Group B: Chemotherapy-related myelosuppression, primary prevention, treatment rate and clinical management1 intervention
Group C: Chemotherapy-induced myelosuppression, secondary prevention, treatment rates, and clinical managemen1 intervention

Trial outcomes

Primary outcomes

1

Incidence of chemotherapy-related myelosuppression and current status of prophylactic therapy

The incidence and treatment status of chemotherapy-related myelosuppression were investigated in the form of questionnaires Like what: 1. Did bone marrow suppression occur after the previous cycle of chemotherapy? (First chemotherapy/occurrence/non-occurrence) 2. Did CIM (chemotherapy-induced myelosuppression) occur during this chemotherapy? (Multiple selections allowed) 3. Survey questions about existing CIM therapeutic drugs

Time frame
2024.09-2025.09

Secondary outcomes

1

Incidence of chemotherapy-related myelosuppression

Through questionnaire survey:the incidence of neutropenia during chemotherapy treatment and the rate of primary and secondary prophylaxis;

Time frame
2024.09-2025.09
2

the rate and economic burden of neutropenia treatment during chemotherapy treatment

Through questionnaire survey:the rate and economic burden of neutropenia treatment during chemotherapy treatment like what:Is there an additional financial burden? A.\<500 yuan, B.500-\<1000 yuan, C.1000-\<3000 yuan, D.≥3000 yuan

Time frame
2024.09-2025.09
3

the incidence of thrombocytopenia and the rate of primary and secondary prevention and treatment during chemotherapy treatment

Through questionnaire survey: the incidence of thrombocytopenia and the rate of primary and secondary prevention and treatment during chemotherapy treatment like what:Is there primary /secondary prevention in this chemotherapy? Yes/No

Time frame
2024.09-2025.09
4

thrombocytopenia treatment rate and economic burden during chemotherapy treatment

Through questionnaire survey: thrombocytopenia treatment rate and economic burden during chemotherapy treatment like what:Does it increase the financial burden of patients to a certain extent? Yes/No

Time frame
2024.09-2025.09

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

The First Affiliated Hospital of Xinxiang Medical College

Lead sponsor

Xinxiang Central Hospital of Henan province

Collaborator

Linzhou People Hospital

Collaborator

Inner Huang County Traditional Chinese Hospital

Collaborator

Changyuan People Hospital

Collaborator

Huojia County People Hospital

Collaborator

Huojia County Alliance Hospital

Collaborator

Qinyang People Hospital

Collaborator

Xinan County People Hospital

Collaborator

Henan Hongli Hospital

Collaborator

Army Hospital of the 83rd Army

Collaborator

Anyang Cancer Hospital

Collaborator

Puyang Hospital of Traditional Chinese Medicine

Collaborator

Puyang Huimin Hospital

Collaborator

Hebi People Hospital

Collaborator

The Second People Hospital of Xinxiang Henan

Collaborator

This trial is not recruiting at the moment. You can still explore other options: