Trial Outcomes & Findings for Additional Neurological Symptoms Before Surgery of the Carotid Arteries - A Prospective Study (ANSYSCAP) (NCT NCT00514592)
NCT ID: NCT00514592
Last Updated: 2013-10-23
Results Overview
Ipsilateral ischemic stroke after the presenting event. Only events that occurs within 90 days and before Carotid EndArterectomy (CEA) is used.
Recruitment status
COMPLETED
Target enrollment
230 participants
Primary outcome timeframe
Before CEA
Results posted on
2013-10-23
Participant Flow
Participant milestones
| Measure |
All Patients
All patients enter the same group
|
|---|---|
|
Overall Study
STARTED
|
230
|
|
Overall Study
COMPLETED
|
230
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Additional Neurological Symptoms Before Surgery of the Carotid Arteries - A Prospective Study (ANSYSCAP)
Baseline characteristics by cohort
| Measure |
All Patients
n=230 Participants
All patients are in the same group
|
|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=5 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
55 Participants
n=5 Participants
|
|
Age, Categorical
>=65 years
|
175 Participants
n=5 Participants
|
|
Sex: Female, Male
Female
|
83 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
147 Participants
n=5 Participants
|
PRIMARY outcome
Timeframe: Before CEAIpsilateral ischemic stroke after the presenting event. Only events that occurs within 90 days and before Carotid EndArterectomy (CEA) is used.
Outcome measures
| Measure |
All Patients
n=230 Participants
All patients enter the same group
|
|---|---|
|
Ipsilateral Ischemic Stroke Before Carotid Endarterectomy
|
33 participants
|
SECONDARY outcome
Timeframe: Before CEASame as primary endpoint, but includes stroke of all types.
Outcome measures
| Measure |
All Patients
n=230 Participants
All patients enter the same group
|
|---|---|
|
Any Stroke Before Carotid Enderarterectomy
|
36 participants
|
Adverse Events
All Patients
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place