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A Randomized Controlled Trial for Evaluating Pain Response in Patients with Spinal Metastases Following Local versus Whole Vertebral Radiotherapy

A Randomized Controlled Trial for Evaluating Pain Response in Patients with Spinal Metastases Following Local versus Whole Vertebral Radiotherapy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023401
Enrollment
Unknown
Registered
2019-05-25
Start date
2019-06-01
Completion date
Unknown
Last updated
2019-05-27

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

Conditions

Spinal Metastases

Interventions

Local radiotherapy group:Intensity modulated radiotherapy for local metastatic lesion
Vertebral radiotherapy group:Intensity modulated radiotherapy for metastatic vertebral

Sponsors

Mianyang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18-80 years; 2) Pathologically confirmed spinal metastatic less than 3 lesions; 3) ECOG score 0-1; KPS =60; 4) without severe hypertension, diabetes, heart disease and so on; 5) There was no contraindication of radiotherapy; Vertebral metastasis in this trail has not received radiotherapy in the past; 6) The estimated survival time is more than 3 months; 7) Patients or family members signed the informed consent; 8) Patients has good compliance with treatment and agreed to cooperate for survival follow-up.

Exclusion criteria

Exclusion criteria: 1) Benign diseases leading to bone destruction; 2) Multiple myeloma and lymphoma and leukemia; 3) Pregnant or lactating women; 4) Patients who underwent radiotherapy or vertebral surgery prior Over the past four weeks to the start of this trial; 5) Severe hypertension, diabetes and heart disease; 6) Severe neurological or psychiatric disorders, including dementia and epileptic seizures; 7) Patients with abnormal coagulation function and risk of fatal massive hemorrhage; 8) Serious adverse reactions are known to occur at any stage of treatment; 9) Those who have participated in other clinical trials in the past four weeks; 10) Researchers believe that some obvious diseases should be excluded from this study.

Design outcomes

Primary

MeasureTime frame
pain-relieving rate;

Secondary

MeasureTime frame
Incidence of side effects;

Countries

China

Contacts

Public ContactYuan Li

Mianyang Central Hospital

yuanli661@163.com+86 18780335867

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 17, 2026