Skip to content

Online adaptive radiotherapy (oART) in radical radiotherapy for cervical cancer — A multi-center randomized controlled study

Online adaptive radiotherapy (oART) in radical radiotherapy for cervical cancer — A multi-center randomized controlled study

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088395
Enrollment
Unknown
Registered
2024-08-19
Start date
2024-08-19
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

cervical cancer

Interventions

IGRT group:IGRT
ART group:oART

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-70 years old; 2.Pathologically confirmed diagnosis of cervical cancer and pathological type of cervical squamous carcinoma; 2018 FIGO staging Ib3, II, IIIC1; 3.Proposed radical pelvic radiotherapy + synchronous sensitising chemotherapy (platinum-based (cisplatin 30-40 mg/m2 or carboplatin alone), starting synchronously in the first week, =5 courses); 4.ECOG score 0-2; 5.Life expectancy greater than 6 months; 6.Ability to remain lying down for more than 30 minutes; 7.Patients were fully voluntary and autonomous and co-operated in signing the study informed consent form; 8.Complete blood count and basal metabolic indexes within 14 days prior to enrolment must meet the following requirements: NEUT = 1.5*109/L, HGB = 60g/L, platelets = 100×109/, blood creatinine < 1.5 mg/dL. AST and ALT are within 2 times the upper limit of normal; 9.Must complete baseline assessments and investigations required prior to treatment before enrolment; 10.be eligible for regular follow-up;

Exclusion criteria

Exclusion criteria: 1.Have received radiotherapy or chemotherapy in the past; 2.Have undergone radical surgery for cervical cancer; 3.Have a previous history of malignant tumour; 4.Pregnant or lactating women; 5.Presence of other serious co-morbidities such as poorly controlled cardiovascular, urinary, digestive, respiratory, haematological and central nervous system diseases; 6.Other conditions deemed unsuitable for participation by the investigator;

Design outcomes

Primary

MeasureTime frame
acute non-haematological toxicity;

Secondary

MeasureTime frame
cCR;Survival and disease progression;

Countries

China

Contacts

Public ContactHu Ke

Peking Union Medical College Hospital

huke8000@163.com+86 10 69154072

Outcome results

None listed

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