Clinical trials

2

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Condition / disease
Location
Status: Not yet recruiting

Study on the Effectiveness and Safety of Two Olive Extract- Based (Olea Europea L. Folium) Supplements, Alone or Combined With a Mullein Extract (Verbascum Thapsus L. Herba Cum Floribus), for the Maintenance of Cognitive Function.

The goal of this clinical trial is to learn if two food supplements based on olive leaf extract, alone or combined with mullein extract, help maintain cognitive function in older adults with mild cognitive impairment (MCI). It will also evaluate their safety. The main questions it aims to answer are: Do the supplements improve or help maintain cognitive function (such as memory and attention)? Do participants experience any side effects when taking the supplements? Researchers will compare two active supplements to a placebo (a look-alike substance with no active ingredients) to see if the supplements are effective. Participants will: Take either one of the two supplements or a placebo every day for 6 months Take 2 capsules per day, preferably between meals, with a small amount of water Visit the clinic at the start of the study, after 3 months, and after 6 months for cognitive assessments Complete questionnaires to evaluate cognitive function and quality of life Be monitored throughout the study for any side effects

Participants needed: 99
Trial details
Age: 60-85Biological sex: AllType: InterventionalSponsor: ISTITUTO FARMOCHIMICO FITOTERAPICO: EPO SRLUpdated: May 14, 2026Locations: 1
Eligibility criteria

aged between 60 and 85 years; [+21]

Status: Recruiting

The Beneficial Effect on the Bowel Function of a Food Supplement Based on Sea Buckthorn (Hippophae Rhamnoides L.) Extract in Subjects With Primary Functional Constipation

The study will aim to evaluate the efficacy and tolerability of a supplementation with Sea Buckthorn (Hippophae rhamnoides L.) at two different dosages for the management of the balance of intestinal function in subjects with primary functional constipation. The primary outcome is the improvement of the frequency of bowel movements (SCBM) in subjects with functional constipation; then the secondary outcomes are the 1) improvement in stool consistency, assessed through the Bristol Stool Form Scale (BSFS) and 2) reduction in the typical symptoms of constipation, such as feeling of bloating and abdominal distension, feeling of heaviness, abdominal pain and flatulence, improving the quality of life of the subjects affected by primary functional constipation.

Participants needed: 135
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: ISTITUTO FARMOCHIMICO FITOTERAPICO: EPO SRLUpdated: Jul 30, 2025Locations: 1
Eligibility criteria

aged between 18 and 70 years [+11]

pregnancy [+3]