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Quantitative Assessment of Pelvic Active Bone Marrow Using mDixon Technique and Its Clinical Application in Radiotherapy for Locally Advanced Rectal Cancer

Quantitative Assessment of Pelvic Active Bone Marrow Using mDixon Technique and Its Clinical Application in Radiotherapy for Locally Advanced Rectal Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127212
Enrollment
Unknown
Registered
2026-06-26
Start date
2026-06-30
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

locally advanced rectal cancer

Interventions

Observation group:None

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Voluntarily sign the informed consent form; 2.Age >= 18 years at enrollment; 3.Eastern Cooperative Oncology Group (ECOG) performance status 0–1; 4.Any sex; 5.Histologically confirmed rectal adenocarcinoma; 6.Diagnosed as stage II–III rectal cancer according to the American Joint Committee on Cancer (AJCC) 8th edition TNM staging system; 7.Has an indication for pelvic radiotherapy; 8.Adequate bone marrow function;

Exclusion criteria

Exclusion criteria: 1.Patients with bone marrow metastases detected by imaging examination; 2.Patients with metallic foreign bodies or artificial hip joint replacements; 3.History of other malignant tumors; 4.Presence of serious diseases (e.g., heart failure or psychiatric disorders); 5.Patients who are pregnant or breastfeeding; 6.Patients concurrently participating in other clinical trials; 7.Patients deemed unsuitable for participation in this study by the investigator;

Design outcomes

Primary

MeasureTime frame
Dose-volume parameters;

Countries

China

Contacts

Public ContactZhang Yaowei

Southern Medical University Southern Hospital

weiyaozhang2@163.com+86 20 62786617

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026