Effect of Alpha-Lipoic Acid Supplementation on the Incidence of Postoperative Atrial Fibrillation in Cardiac Surgery Patients

Sponsor
Ain Shams University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06151652
Collaborator
(none)
350
1
2
4
87.3

Study Details

Study Description

Brief Summary

ALA is administered orally since it is without difficulty absorbed in the stomach. ALA goes through the blood brain barrier and does not show toxic effects and actions at doses used for prophylactic and therapeutic purposes. This has encouraged us to use an efficient anti-oxidant and anti-inflammatory agent, alpha-lipoic acid (biochemical) as a relevant option to prevent POAF.

Condition or Disease Intervention/Treatment Phase
  • Drug: Alpha Lipoic Acid 600 MG Oral Tablet
  • Drug: Placebo
Phase 4

Detailed Description

Investigators computed on the basis of findings from a prior study found the incidence of POAF after cardiac surgery of about 25% . Assuming a slightly lower alpha-lipoic acid' effect to previous study. If the true relative risk of AF for experimental subjects relative to controls is 0.5 , with α equivalent to 0.5 and power (1 - β) is 0.8, the estimated sample size is 152 experimental subjects and 152 control subjects in order to be able to reject the null hypothesis that this relative risk equals 1 with probability (power) of 0.8. investigators used the uncorrected chi-squared statistics to evaluate this null hypothesis. STATA software version and taking into account a possible dropout of 15%, the total sample size was: 304 + 0.15 (304) × 2 = 350 subjects of which there will be 175 controls and 175 experimental subjects %, assuming an enrolment ratio of 1:1.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
350 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Prevention
Official Title:
Effect of Alpha-Lipoic Acid Supplementation on the Incidence of Postoperative Atrial Fibrillation in Cardiac Surgery Patients
Anticipated Study Start Date :
Dec 1, 2023
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
Apr 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Group 1 (Control group, N = 175 patients)

which will include patients adopted to the hospital standard of care.

Drug: Placebo
placebo

Active Comparator: Group 2 (Test group, N = 175 patients)

which will include patients who will receive Alpha-lipoic acid (Thiotacid 600 mg ®) at a dose of 600 mg three times daily for one day prior to surgery, followed by Alpha-lipoic acid 600 mg twice daily for 5 days post-surgery plus the standard care.

Drug: Alpha Lipoic Acid 600 MG Oral Tablet
Alpha-lipoic acid (Thiotacid 600 mg ®) at a dose of 600 mg three times daily for one day prior to surgery, followed by Alpha-lipoic acid 600 mg twice daily for 5 days post-surgery plus the standard care.

Outcome Measures

Primary Outcome Measures

  1. • Number of Participants with POAF [1 month]

Secondary Outcome Measures

  1. Total intensive care unit length-of-stay [3 months]

    number of days at intensive care unit

  2. Total hospital length-of-stay [3 months]

    number of days at hospital

  3. 30 days mortality [1-month]

    deaths number

  4. Serum creatinine [5 days]

    creatinine level

  5. Major adverse cardiovascular outcomes [1 month]

    (Myocardial injury - Stroke - Permanent pacemaker - Pericardial effusion and pleural effusion- Bleeding)

  6. Duration of ventilation [5 days]

    hours needed to remove ventilator

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • I

  • Male or female patients above 18 years of age who are scheduled for cardiac surgery.

Exclusion Criteria:
  • Any urgent or emergency surgery.

  • Poor Left ejection volume (EF < 30%).

  • Intake of steroids or any antiarrhythmic drugs except beta blockers during the last month before surgery

  • Unable or unwilling to provide informed written consent.

  • Pregnancy or lactation

  • Known hypersensitivity to the study drug.

  • Current treatment with antioxidants or alpha-lipoic acid for any indication.

  • Infection or inflammatory disease except coronary artery disease.

  • Left atrium size >70 mm.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ain shams university Cairo Egypt

Sponsors and Collaborators

  • Ain Shams University

Investigators

  • Study Director: Marwa Adel, PhD, Ain Shams University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ain Shams University
ClinicalTrials.gov Identifier:
NCT06151652
Other Study ID Numbers:
  • ALA post cardiac surgery
First Posted:
Nov 30, 2023
Last Update Posted:
Nov 30, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 30, 2023