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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03798665
Other study ID # CB-RWS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 6, 2018
Est. completion date July 6, 2019

Study information

Verified date January 2019
Source Af?liated Hospital of North Sichuan Medical College
Contact Xian Bang Tan
Phone 13458406996
Email tbx-n9mB@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Prospective, multicenter, non-interventional registration studies were used in this project . Eight hundreds patients with solid tumors who met the inclusion criteria in six hospitals in Sichuan Province, Sichuan Province, were selected from the first chemotherapy cycle using PEG-rhG-CSF (can be any chemotherapy cycle of the patient), and each subsequent chemotherapy cycle was recorded. The use of PEG-rhG-CSF and related patient outcomes until the end of chemotherapy. Analyze the clinical practice of using PEG-rhG-CSF in the real world.


Recruitment information / eligibility

Status Recruiting
Enrollment 800
Est. completion date July 6, 2019
Est. primary completion date July 6, 2019
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Age = 18 years old;

2. Diagnosed as a malignant solid tumor by histology and cytology, requiring chemotherapy patients;

3. The first use of PEG-rhG-CSF during the chemotherapy cycle (not limited to the first chemotherapy cycle, can be any chemotherapy cycle of the patient);

4. Subjects volunteered to participate in this clinical trial and signed informed consent.

Exclusion Criteria:

1. PEG-rhG-CSF was used in the current chemotherapy cycle;

2. Have received hematopoietic stem cell transplantation or bone marrow transplantation;

3. Other drug clinical trials are currently underway.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Pegfilgrastim(PEG-rhG-CSF)
From the first chemotherapy cycle using PEG-rhG-CSF (which can be any chemotherapy cycle of the patient), record the use of PEG-rhG-CSF in this cycle and each subsequent chemotherapy cycle, including dosage, administration time and dosing frequency

Locations

Country Name City State
China Affiliated Hospital of North Sichuan Medical College Nanchong Sichuan

Sponsors (1)

Lead Sponsor Collaborator
Af?liated Hospital of North Sichuan Medical College

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Dosage of PEG-rhG-CSF in chemotherapy 1 YEAR
Primary Administration time of PEG-rhG-CSF in chemotherapy 1 YEAR
Primary dosing frequency of PEG-rhG-CSF in chemotherapy 1 YEAR
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