Trials / Completed
CompletedNCT00519337
Impact of Ascorbic Acid on Post-Cardiothoracic Surgery Inflammation
The Impact of Ascorbic Acid Therapy on Inflammatory Mediators in Cardiothoracic Surgery Patients: The Atrial Fibrillation Suppression Trial IV (AFIST IV) Pilot Study
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 25 (actual)
- Sponsor
- Hartford Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to see if ascorbic acid (Vitamin-C) therapy will reduce inflammation following heart surgery.
Detailed description
Atrial Fibrillation is a significant cause of morbidity following cardiothoracic surgery. Despite prophylactic therapy with beta-blockers and amiodarone, post-operative atrial fibrillation occurs in approximately 22% of patients. We believe that by reducing the inflammation that is caused during CTS, we can see further improvements without any negative effects on hemodynamics. Ascorbic acid, a free radical scavenger has been found to lower inflammation mediators but never in a CTS population. This study will help determine the affect of ascorbic acid on the inflammation associated with CTS.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ascorbic acid | Ascorbic acid, 2 g p.o. the night before surgery followed by 500mg B.I.D. for 4 post-operative days |
| DRUG | Placebo | Placebo capsule, 4 capsules the night before surgery followed by 1 capsule B.I.D. for 4 postoperative days |
Timeline
- Start date
- 2008-10-01
- Primary completion
- 2009-10-01
- Completion
- 2011-04-01
- First posted
- 2007-08-22
- Last updated
- 2012-01-05
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00519337. Inclusion in this directory is not an endorsement.