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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03880149
Other study ID # MeirMc0242-18CTIL
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 1, 2020
Est. completion date June 1, 2021

Study information

Verified date September 2020
Source Meir Medical Center
Contact Dan Nemet, MD
Phone 972-9-7471640
Email Dan.Nemet@clalit.org.il
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study will examine the association between omega-3 status and the effects of omega-3 supplementation on changes in tendon structure and recovery from tendon injuries and inflammatory markers in competitive athletes. Half of the participants will receive omega-3 in combination with vitamin E, while the other half will receive a placebo and vitamin E.


Description:

Sports injuries are common among athletes, while injury prevention received much clinical attention, there is no consensus among clinicians and researchers as to which injury-causing factors are dominant. It has been suggested that increased training load may be the leading cause of sports injuries, since tendons are sensitive to changes in load, making them vulnerable to injury. Inflammation is one of the reversible risk factors to sports injuries, and there are numerous methods which are used to treat inflammation. It has been recently suggested that inflammation reactions are affected by Omega-3 status and that omega-3 deficiency may increase the risk of sports and tendon injuries. The omega-3 fatty acid may act as a regulator of membrane structure and function, intracellular signaling pathways, transcription factor activity, and gene expression and reducing inflammation. Due to these functions, omega-3 may influence exercise-induced injuries/inflammation in athletes, thus, may influence their health and allowing training.


Recruitment information / eligibility

Status Recruiting
Enrollment 140
Est. completion date June 1, 2021
Est. primary completion date June 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

Part one:

- Training for at least 5 hours per week.

- No complaints about lower extremities pains during the last 12 months.

Part two:

- Training for at least 5 hours per week.

- Diagnosed with patellar and Achilles tendinitis.

Exclusion Criteria:

- Underwent lower extremities surgeries.

- Allergic to Fish products.

- Athletes who use anti-inflammatory drugs and/or omega-3 supplements.

- Pregnant and/or nursing mothers.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Omega-3
Each omega-3 capsule contains 600 mg, including 400 mg EPA + 200 mg Docosahexaenoic acid (DHA) and 400 IU of vitamin E for 5 omega-3 capsules. Omega-3 dosage: 1 g per 15 kg body mass
Other:
Placebo
Medium-chain triglyceride (MCT) and vitamin E

Locations

Country Name City State
Israel Wingate institute Netanya

Sponsors (3)

Lead Sponsor Collaborator
Meir Medical Center Tel Hai College, University of Haifa

Country where clinical trial is conducted

Israel, 

References & Publications (4)

Black KE, Witard OC, Baker D, Healey P, Lewis V, Tavares F, Christensen S, Pease T, Smith B. Adding omega-3 fatty acids to a protein-based supplement during pre-season training results in reduced muscle soreness and the better maintenance of explosive pow — View Citation

Da Boit M, Hunter AM, Gray SR. Fit with good fat? The role of n-3 polyunsaturated fatty acids on exercise performance. Metabolism. 2017 Jan;66:45-54. doi: 10.1016/j.metabol.2016.10.007. Epub 2016 Oct 26. Review. — View Citation

Lewis EJ, Radonic PW, Wolever TM, Wells GD. 21 days of mammalian omega-3 fatty acid supplementation improves aspects of neuromuscular function and performance in male athletes compared to olive oil placebo. J Int Soc Sports Nutr. 2015 Jun 18;12:28. doi: 1 — View Citation

von Schacky C, Kemper M, Haslbauer R, Halle M. Low Omega-3 Index in 106 German elite winter endurance athletes: a pilot study. Int J Sport Nutr Exerc Metab. 2014 Oct;24(5):559-64. doi: 10.1123/ijsnem.2014-0041. Epub 2014 Sep 8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Tendon Structure Changes in the echo pattern of patellar and Achilles tendons structure using Ultrasound Tissue Characterization (UTC). Distribution (%) of echo type 1-3. 6 months
Secondary Inflammatory marker Serum interleukin 6 (IL-6) (pg/mL) 3 months
Secondary Muscle Strength Total work (Kjoule) (using Biodex isokinetic testing protocol) 6 months
Secondary Omega-3 status Distribution (%) of 26 identified fatty acids - measured in Blood 6 months
Secondary Cross sectional area of Achilles tendon measured using Ultrasound Tissue Characterization (UTC) (cm^2) 6 months
Secondary Range of motion - knee using digital inclinometer for range of motion measurement (degrees) 6 months
Secondary Pain assessment pain severity using visual analog scale (VAS) - on a scale of 0 -10, 0 being no pain and 10 the worst pain ever 6 months
Secondary functional assessment VISA P questionnaire - scale 0-100 3 months
Secondary Pro-inflammatory cytokine. Serum interleukin 17 (IL-17) (pg/mL) 3 months
Secondary Marker for inflammation C Reactive Protein (CRP) (mg/L) 3 months
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