Clinical trial · Interventional
Comparison of Set-up Reproducibility Between Prone and Supine Intensity Modulated Radiotherapy (IMRT) for the Adjuvant Treatment of Breast Carcinoma After Lumpectomy
NCT00887692CI-TRIAL-00004037completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
10 patients will be treated alternating daily between prone and supine position for breast radiotherapy to compare set-up accuracy. Prone treatment will be given on the odds days and supine treatment on the even days.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Carcinoma | Breast Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| prone and supine position | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Random set-up error
- timeFrame
- daily during radiotherapy
Secondary outcomes (4)
- measure
- Systemic set-up error
- timeFrame
- daily during radiotherapy
- measure
- Respiration-related motion amplitude
- measure
- time of treatment delivery
- timeFrame
- daily during radiotherapy
- measure
- Dose-volume parameters
- timeFrame
- of planning
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * female patients * multidisciplinary decision of adjuvant radiotherapy after lumpectomy for breast cancer * minimum 18 years * informed consent obtained, signed and dated before specific protocol procedures. Exclusion Criteria: * mastectomy * need for axillary irradiation * bilateral breast irradiation * previous irradiation at the same time * pregnant or breastfeeding * mental condition rendering the patient unable to understand the nature, scope and possible consequences of the study. * patient unlikely to comply with the protocol; i.e. uncooperative attitude, inability to return for follow-up visits, and unlikely to complete the study.
References
Publications (0)
Data not yet available
No reference posted for this study.