EUCTR2013-001447-31-GB
Active, not recruiting
Phase 1
A randomised controlled trial to study the effect of acetazolamide on the incidence of blood-stained CSF, effect on cerebrospinal fluid (CSF) pressure, CSF drainage and neurological dysfunction in patients undergoing thoracic-abdominal aortic intervention. - Acetazolamide in aortic surgery
iverpool Heart and Chest Hospital NHS Foundation Trust0 sites60 target enrollmentOctober 29, 2013
DrugsDiamox
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- iverpool Heart and Chest Hospital NHS Foundation Trust
- Enrollment
- 60
- Status
- Active, not recruiting
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Elective patients who have given consent and are 18\+ years
- •\- Patients able to comply with the pre\-operative course of acetazolamide treatment (treatment group) and who have had a blood sample collected at least three days prior to surgery
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range 40
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range 20
Exclusion Criteria
- •\- Non\-elective patients, who were not able to participate in pre\-operative acetazolamide treatment and blood sample tests three days prior to surgery
- •\- Patients without consent
- •\- Patients under the age of 18
- •\- Patients unable to independently comprehend and complete the consent form
- •\- Patients unable to independently comply to the pre\-operative course of acetazolamide treatment
Outcomes
Primary Outcomes
Not specified
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