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

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

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 CEA

Ipsilateral ischemic stroke after the presenting event. Only events that occurs within 90 days and before Carotid EndArterectomy (CEA) is used.

Outcome measures

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 CEA

Same as primary endpoint, but includes stroke of all types.

Outcome measures

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

Dr Elias Johansson

UmeƄ University

Phone: +46907850000

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place