NCT05022641 · ADVERSE EVENTS
Adverse events
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
Adverse events occurred during the study; they are not necessarily caused by treatment. Serious events are not interchangeable with severe/grade 3–4 events. These safety populations may differ from efficacy populations.
- Collection time frame
- Up to 6-months after surgery.
- Other-event reporting threshold
- 0%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| PTeye | 0 / 81 | 0 / 81 | 0 / 81 |
| Standard of Care | 0 / 79 | 0 / 79 | 0 / 79 |
Serious adverse events
Other reported adverse events
Complete source fields
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 81
- description
- The surgeon will use the PTeye as an intraoperative tool to identify if a suspect tissue is a parathyroid or not, during the parathyroid surgery. PTeye: The surgeon will first take 5 baseline NIRAF measurements on the thyroid gland (or neck muscle, if thyroid is absent) using the disposable sterile fiber probe that is connected to the PTeye console (see Figure 1), as per device functionality requirements.
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 81
- serious Num Affected
- 0
- serious Num At Risk
- 81
- title
- PTeye
- deaths Num Affected
- 0
- deaths Num At Risk
- 79
- description
- The surgeon will rely solely on her/his surgical experience in identifying the parathyroid glands during the operations.
- id
- EG001
- other Num Affected
- 0
- other Num At Risk
- 79
- serious Num Affected
- 0
- serious Num At Risk
- 79
- title
- Standard of Care
- frequency Threshold
- 0
- time Frame
- Up to 6-months after surgery.
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Preserved source evidence · Not medical advice
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