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Carboplatin Allergy Score to Prevent Severe Platinum Allergy before Carboplatin Chemotherapy in Patients with Recurrent Gynecologic Tumors

Carboplatin Allergy Score to Prevent Severe Platinum Allergy before Carboplatin Chemotherapy in Patients with Recurrent Gynecologic Tumors

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034534
Enrollment
Unknown
Registered
2020-07-08
Start date
2020-07-08
Completion date
Unknown
Last updated
2020-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent gynecological malignant tumor

Interventions

High-risk group:Desensitization
Middle-risk group:Monitoring
Low-risk group: Guanchá 2/5000 Observed

Sponsors

Shengjing Hospital Affiliated to China Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) The patient is completely voluntary and autonomous, and signs the research informed consent before entering the group; 2) Histopathology confirmed the recurrence of gynecological malignant tumors; 3) Proposed carboplatin chemotherapy; 4) Aged >= 18 years old and = 12 weeks; 7) Renal function (within the normal range of serum creatinine value); liver function (with AST and ALT within 2 times the upper limit of normal, within the normal range of bilirubin); bone marrow function (leukocytes > 3.0*10^9/L; neutral Granulocytes > 1.5 * 10^9/L; platelets > 100 * 10^9/L; Hb > 80g/L).

Exclusion criteria

Exclusion criteria: 1) Past (within 5 years) or suffering from other uncured malignant tumors; 2) Patients with congenital diseases and infectious diseases; 3) Past or present patients with heart disease class II or above according to the New York Heart Association (NYHA) or patients with congestive heart failure; 4) The investigator believes that it will affect the subject's ability to receive the research program treatment of uncontrolled serious medical diseases, such as combined with serious medical diseases, including severe heart disease, cerebrovascular disease, uncontrolled diabetes, uncontrolled high Blood pressure, uncontrolled infections, active peptic ulcers, etc.; 5) Patients who have experienced severe allergic symptoms with platinum in the past; 6) Patients with central nervous system disease or central nervous system metastasis; 7) The investigator judges that it is not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Allergy classification;Incidence and severity of anaphylaxis;

Countries

China

Contacts

Public ContactXiuqin Li

Shengjing Hospital Affiliated to China Medical University

lixq@sj-hospital.org+86 18940251286

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026