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NCT06203223

The Effect of Ovamax on Oocyte Quality

Terminated NA Last updated 20 May 2025
What this trial tests

NA trial testing Ova-max in Female in 97 participants. Terminated before completion.

Timeline
1 July 2021
Primary endpoint
30 November 2024
15 January 2025

Quick facts

Lead sponsorAristotle University Of Thessaloniki
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment97
Start date1 July 2021
Primary completion30 November 2024
Estimated completion15 January 2025
Sites1 location across Greece

Drugs / interventions tested

Conditions studied

Sponsor

Aristotle University Of Thessaloniki

Who can join

Adults 18 to 46, female only, with Female or Infertility. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Oocyte quality is a basic parameter that affects embryo quality and therefore it influences the outcome of assisted reproduction. It has been suggested that oocyte quality is improved by the intake of vitamins and antioxidants. Ova-Max is a dietary supplement that consists of vitamins, minerals and antioxidants which improve women's oocytes by preventing oxidative stress. Specifically, Ovamax includes Chasteberry, Melatonin, Myo-Inositol, Folic Acid, Co-Enzyme Q10, Vitamin E, L-Arginine, Grape seed extract and Alpha-lipoic Acid. The purpose of this study is to evaluate the influence of Ova-max intake on oocyte quality in women undergoing In Vitro Fertilization. According to the research hypothesis the administration of Ova-Max for three months increases oocyte quality in women undergoing intracellular sperm injection after ovarian stimulation and oocyte retrieval.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Female

Currently open trials in the same condition.

Other Aristotle University Of Thessaloniki trials

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06203223.

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