Trial · NCT07887048
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 14 of 14
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Proportion of patients with setups performed in sitting position for which all interfraction shifts are below 3 mm in all 3 directions and 3 anatomical subregions | From enrollment to the end of follow up at 8 months | |
| Secondary | Proportion of patients with all the measurements below 3 mm in each anatomical subregion | From enrollment to the end of follow up at 8 months | |
| Secondary | Variability of the inter fraction motion (quantitative values) measured at each setup | From enrollment to the end of follow up at 8 months | |
| Secondary | Variability of the intra fraction motion from optical images during the first 2 weeks for the chin, neck and shoulders over a 21-min period | From enrollment to the end of follow up at 8 months | |
| Secondary | Likert scale about satisfaction and comfort in both positions. | From enrollment to the end of follow up at 8 months | |
| Secondary | Interruption is defined by the number of times where the patient will request to remove the thermoplastic mask during the beam delivery or the treatment simulation. | From enrollment to the end of follow up at 8 months | |
| Secondary | Difference in motion illness symptoms measured before and after upright test based on the motion illiness symptoms classification | From enrollment to the end of follow up at 8 months | |
| Secondary | Difference between the result of the distress thermometer in supine and in sitting position | From enrollment to the end of follow up at 8 months | |
| Secondary | Rate of patients with dysphagia based on the PRO-CTCAE on difficulty swallowing | From enrollment to the end of follow up at 8 months | |
| Secondary | Number of patients who accepted to be setup on the chair and tolerate the simulation of the treatment. | From enrollment to the end of follow up at 8 months | |
| Secondary | Time between the moment when the patient is ready to setup and before acquisition of reference images. (in minutes) | From enrollment to the end of follow up at 8 months | |
| Secondary | Time between the moment when the patient is ready to setup and before images verification (in minutes). | From enrollment to the end of follow up at 8 months | |
| Secondary | Time between the moment when RTT is close to the patient and the patient is in standing position (in minutes). | From enrollment to the end of follow up at 8 months | |
| Secondary | Number of interruptions in supine and sitting position during the beam delivery or the treatment simulation | From enrollment to the end of follow up at 8 months |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT07887048/registered