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The radiotherapy guided by DIBH based on VSM technology of United-Imaging 506c accelerator

The radiotherapy guided by DIBH based on VSM technology of United-Imaging 506c accelerator

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110333
Enrollment
Unknown
Registered
2025-10-13
Start date
2025-10-30
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Tumors of the chest and upper abdomen

Interventions

Chest and upper abdominal tumor group:Carry out stereotactic radiotherapy guided by the VSM-DIBH technology

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Tumor types: liver metastases, pancreatic cancer, and other upper abdominal tumors (near the diaphragm); 2. Respiratory control ability: the patient can independently perform deep inspiration breath-hold (DIBH) maneuvers, with a breath-hold time of >=20 seconds and respiratory amplitude fluctuation <=3mm (monitored via the VSM system); 3. Anatomical stability: target volume <=5cm, without significant pleural or abdominal effusion or diaphragm adhesion; 4. The investigator judges, based on the subject's medical history, physical examination, and vital signs, that their general health status is suitable.

Exclusion criteria

Exclusion criteria: 1. Respiratory dysfunction: Acute stage of COPD, severe impairment of lung function (FEV1 < 50% of predicted value) or inability to perform breath-holding training; 2. Positional restrictions: Unable to lie flat or maintain a fixed position (such as severe spinal deformity); 3. Suffering from uncontrollable comorbid diseases, including but not limited to symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, arrhythmia, active peptic ulcer or bleeding disorders; 4. Patients with patent foramen ovale; 5. Patients unable to cooperate with continuous follow-up.

Design outcomes

Secondary

MeasureTime frame
Acute toxic reaction;Progression-free survival, PFS;

Primary

MeasureTime frame
3-month effective rate;

Countries

China

Contacts

Public ContactWang Hao

Peking University Third Hospital

hhbysy@126.com+86 186 1120 7267

Outcome results

None listed

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