ROTEM and Dietary Supplements

Sponsor
University of Pretoria (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03125551
Collaborator
(none)
0
5
2

Study Details

Study Description

Brief Summary

Dietary Supplements can affect platelet activation and aggregation, which could result in bleeding tendencies. This study wishes to evaluate the influence that these supplements has on platelet function using Rotational thromboelastometry.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Ginger
  • Dietary Supplement: Garlic
  • Dietary Supplement: Ginkgo Biloba
  • Dietary Supplement: Ginseng
  • Other: Placebo
N/A

Detailed Description

The WHO informs us that more than 80% of patients in Africa use traditional/herbal medicines as their primary source of health care. The Mayo Clinic stated that nearly 40% of adults reported using complementary and alternative medicine (CAM). Many of these herbal medicines as well as dietary supplements have effects on the coagulation cascade and have been identified as such using laboratory tests including aPTT, PT, INR, light transmission aggregometry and impedence aggregometry to mention but a few.

This study wishes to evaluate coagulation abnormalities using viscoelastic point-of-care coagulation monitoring in this population. This test is readily available in large hospitals and academic settings and is increasingly being used in perioperative medicine. It provides information on coagulation and thrombolysis with minimal delay when compared to other laboratory-based coagulation tests.

The dietary supplements which will be evaluated in this study are ginger, garlic, gingko biloba and ginseng. These four herbal supplements were identified as the most commonly used substances known to modulate the coagulation system. These herbal supplements will be investigated within their maximum daily allowance dosages.

A five-armed placebo-controlled study will be undertaken and study subjects will be recruited on a volunteer basis. Subjects will be divided into five groups and each group will receive one of the four dietary supplements and the fifth group placebo, for a two week period. Rotational thromboelastometry (ROTEM) studies will be performed on blood samples obtained from each participant at baseline and at the end of the treatment period to identify coagulation abnormalities. Most of these herbal medicines have been identified to affect platelet function and this study will specifically look at platelet function determined by maximum clot firmness (MCF) in the ROTEM analysis.

Viscoelastic point-of-care coagulation monitoring in patients using herbal medicines and dietary supplements will aid decision making regarding cause of perioperative haemorrhage and need for specific blood products. It will therefore assist with goal-directed management of perioperative haemorrhage. It will also aid the anaesthetist wishing to employ a regional anaesthetic technique in this patient group.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Five- armed, placebo- controlled ( 4 intervention groups and 1 placebo group)Five- armed, placebo- controlled ( 4 intervention groups and 1 placebo group)
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
Each participant will be blinded to the dietary supplement which they will be taking. The medical technologist doing the ROTEM will be blinded to the dietary supplements as well.
Primary Purpose:
Diagnostic
Official Title:
Viscoelastic Point-of-Care Coagulation Monitoring and Dietary Supplements: A Randomized, Double-blind, Placebo-controlled Trial
Anticipated Study Start Date :
Jun 1, 2017
Anticipated Primary Completion Date :
Jul 1, 2017
Anticipated Study Completion Date :
Aug 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Ginger

Ginger ( Zingiber officinale) 4 grams po dly for 14 days

Dietary Supplement: Ginger
Ginger dosage at daily recommended allowance

Active Comparator: Garlic

Garlic (Allium sativum) 4-12 mg alliin po dly for 14 days

Dietary Supplement: Garlic
Garlic dosage at daily recommended allowance

Active Comparator: Ginkgo Biloba

Ginkgo Biloba 40mg po tds for 14 days

Dietary Supplement: Ginkgo Biloba
Ginkgo Biloba dosage at daily recommended allowance

Active Comparator: Ginseng

Ginseng 400mg po dly for 14 days

Dietary Supplement: Ginseng
Ginseng dosage at daily recommended allowance

Placebo Comparator: Placebo

Placebo po dly for 14 days

Other: Placebo
Daily dosage strategy

Outcome Measures

Primary Outcome Measures

  1. Platelet dysfunction determined by ROTEM when consuming ginger, garlic, ginkgo biloba and ginseng. [2-4 weeks]

    To determine if viscoelastic point-of-care coagulation monitoring (ROTEM) detects abnormalities in platelet function when subjects consume ginger, garlic, ginkgo biloba and ginseng within their recommended daily allowances. ExTEM and FibTEM analysis will be performed and difference in MCF values will determine if there is platelet dysfunction or not.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Age 18-60 years

  2. Both males and females

  3. Healthy volunteers

  4. Smokers and Non-smokers

  5. Staff frequenting the theatre complex at Steve Biko Academic Hospital

Exclusion Criteria:
  1. Use of any medication, excluding oral contraceptive pills, in the two week period prior to commencement of the study. Medicines excluded, include aspirin, dietary supplements, herbal teas, anticoagulants and other non-steroidal anti-inflammatory medications. . Oral contraceptive pills were omitted as an exclusion criteria, taking into account that the majority of woman use these. The results of the study will be a better reflection of the effect of these dietary supplements in the modern day woman. Its coagulant properties will be taken into account during data analysis.

  2. History of any chronic medical or psychiatric illness.

  3. Current excessive alcohol intake - more than 14 units a week in woman and more than 21 units a week in men.

  4. Pregnant or lactating mothers.

  5. Possible planned surgery during the study period

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Pretoria

Investigators

  • Principal Investigator: Jayde V Wyngaard, MBCHB, University of Pretoria

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jayde Wyngaard, Dr, University of Pretoria
ClinicalTrials.gov Identifier:
NCT03125551
Other Study ID Numbers:
  • MMed Anaesthesiology -15402364
First Posted:
Apr 24, 2017
Last Update Posted:
May 9, 2018
Last Verified:
May 1, 2018
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
Keywords provided by Jayde Wyngaard, Dr, University of Pretoria
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 9, 2018