Sea Buckthorn trials recruiting now

1 registration that name sea Buckthorn as a study arm and are recruiting or about to, as ClinicalTrials.gov listed them on Oct 20, 2026. Read each listing for its full criteria and current status.

Kymata never assesses eligibility. Each listing names its own criteria; only its study team can say whether someone can join. Trial doses are given under the trial's monitoring and are not a schedule for anyone outside it.

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All 1 registrations

RecruitingNCT07082673

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

  • No phase
  • ISTITUTO FARMOCHIMICO FITOTERAPICO: EPO SRL
  • About 135 people
  • Started Jul 24, 2025

In plain words A study of sea Buckthorn in people 18 to 70, run by ISTITUTO FARMOCHIMICO FITOTERAPICO: EPO SRL. It plans to enroll about 135 people at 1 site, none in the US.

Who it lists and where

Who the trial lists, as registered

Lists people 18 to 70. Conditions: Functional Constipation (FC).

  • aged between 18 and 70 years
  • able to understand and sign informed consent
  • HIV negative test
  • negative pregnancy test

9 more inclusion criteria and the exclusion criteria are on the listing.

What it tests, as registered

Sea Buckthorn (Hippophae rhamnoides L.) botanical extract 500 mg.; Sea buckthorn (Hippophae rhamnoides L.) 1500 mg.; Placebo

Registered summary

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 full summary is on the listing.

Where, as registered

No US site; Italy (1).

ClinicalTrials.gov lists 2 open registrations for this search, including ones where sea Buckthorn is not a study arm or that are past the 1 we keep. Search them on ClinicalTrials.gov (opens in new tab).

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