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Homeopathy for Prevention of Atrial Fibrillation After Aortocoronary Bypass Surgery

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Medical University of Vienna

Status and phase

Terminated
Phase 4

Conditions

Atrial Fibrillation

Treatments

Drug: Nux vomica (active comparator)
Drug: Placebo (placebo comparator)

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

After heart surgery, about 30% of patients suffer from atrial fibrillation. Patients are randomized into two groups receiving either potentized Strychnos Nux vomica or placebo under double blind conditions. Postoperatively, ECGs are done to monitor cardiac rhythm.

Full description

Preoperatively, patients receive potentized Nux vomica or placebo sublingually. Then, patients are observed regarding atrial fibrillation postsurgical. The difference between the group of patients with and without nux vomica is recorded.

Enrollment

12 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients before elective Heart valve - or aortocoronary by pass surgery with heart-lung-machine.

Exclusion criteria

  • Pregnant patients
  • Patients with preoperative atrial fibrillation and/or hyperthyreosis

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

12 participants in 2 patient groups, including a placebo group

Placebo globules group
Placebo Comparator group
Description:
Patients receive Placebo globules made out of sugar and looking similar to active drug sublingually before surgery.
Treatment:
Drug: Placebo (placebo comparator)
Nux vomica group
Active Comparator group
Description:
Patients receive Nux vomica globules made out of sugar sublingually before surgery.
Treatment:
Drug: Nux vomica (active comparator)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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