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A randomized controlled trial of Nedaplatin versus Cisplatin concurrent chemoradiotherapy in patients with cervical cancer

A randomized controlled trial of Nedaplatin versus Cisplatin concurrent chemoradiotherapy in patients with cervical cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017108
Enrollment
Unknown
Registered
2018-07-12
Start date
2018-09-01
Completion date
Unknown
Last updated
2022-02-01

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

Conditions

cervical cancer

Interventions

AA:nidaplatin
B:cisplatin

Sponsors

Shanghai Jiao Tong University Affiliated Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with cervical cancer diagnosed by pathology for the first time; 2. According to the 2014 FIGO cervical cancer stage, patients with stage IB-IVa; 3. Aged 18 to 70 years; 4. ECOG general condition score 0-2, weight loss = 80 mL / min; (3) Blood function: absolute neutrophil count (ANC) >= 2 x 10^9 / L, platelet count >= 100 x 10^9 / L and hemoglobin >= 9g / dL; (4) Blood sugar level: good blood sugar control, fasting blood glucose 3.9-7.2mmol / L, postprandial blood glucose = 10.0mmol / L, HbA1c < 7% (China Type 2 Diabetes Prevention Guide 2010 edition). 11. The subject agrees and signs the informed consent form (if the subject does not have the ability to judge, the legal guardian is required to sign the informed consent form).

Exclusion criteria

Exclusion criteria: 1. With a serious uncontrollable infection; 2. Factors affecting drug delivery, distribution, metabolism, excretion, etc., such as mental disorders, central nervous system abnormalities, chronic diarrhea, ascites, pleural effusion, etc.; At the same time, receive experimental treatment from other clinical studies (in the treatment period of clinical research or participate in other drug clinical trials within 30 days); 3. Long-term use of immunosuppressants after organ transplantation or combined use of immunopotentiators; 4. There are severe heart, lung, liver and kidney dysfunction such as decompensated heart, lung, kidney, liver and other major organ dysfunction, failure or poor glycemic control, can not tolerate radiotherapy and chemotherapy; 5. Patients with cognitive dysfunction, or who have been judged by the investigator to have poor compliance with radiotherapy and chemotherapy.

Design outcomes

Primary

MeasureTime frame
Hematology routine;Adverse effects;

Secondary

MeasureTime frame
local recurrence;

Countries

China

Contacts

Public ContactYang Xiaojing

Shanghai Jiao Tong University Affiliated Sixth People's Hospital

yangxj717@163.com+86 13818105740

Outcome results

None listed

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