Clinical trial Recruiting at 1 site Interventional Ages 18 to 50 Women only

Sea buckthorn infusion for body composition in overweight women

Official title: Sea Buckthorn Aqueous Infusion Impact on Body Composition Metrics Among Overweight Female Adults.

Run by University of Veterinary and Animal Sciences, Lahore - Pakistan · NCT07313423 · Data updated 2026-11-12

This study will test if drinking a daily 5 g sea buckthorn aqueous infusion for 12 weeks helps lower weight, BMI, waist‑hip ratio, and visceral fat in overweight women aged 18–50.

Quick facts

Study typeInterventional
Ages18 Years to 50 Years
SexWomen only
Enrollment60 (estimated)
SponsorUniversity of Veterinary and Animal Sciences, Lahore - Pakistan
Academic / other
Locations1 site (Lahore, Punjab Province)
StatusRecruiting
StartedJanuary 1, 2026
Main results expectedMarch 30, 2026
Study endsApril 15, 2026
Registry record updatedJanuary 2, 2026
Trial IDNCT07313423 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Women aged 18–50 with BMI 25–29.9 kg/m² who are not pregnant or lactating, do not have chronic metabolic or gastrointestinal disease, are not using weight‑loss drugs or supplements, and do not smoke or drink alcohol are ideal candidates.

Probably not a fit

People outside the enrolled profile—men, those with BMI below 25 or ≥30, pregnant or breastfeeding women, those with chronic metabolic/GI conditions, high physical activity (>1.4), or on weight‑loss medications—are unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Sixty overweight women (BMI 25–29.9 kg/m²) will be randomized 1:1 to a daily 5 g sea buckthorn aqueous infusion taken each morning for 12 weeks or to continue usual habits without supplementation. The infusion is prepared fresh each day by dispersing 5 g sea buckthorn powder in 250 mL lukewarm boiled water and consumed after breakfast. Body composition (weight, BMI, waist‑hip ratio, visceral fat) will be measured at baseline and follow-up using an InBody 270 bioelectrical impedance analyzer. Data will be analyzed using standard statistical methods (ANOVA) to compare changes between groups.

Why it matters

Potential benefit: If effective, the infusion could offer a simple, low‑cost dietary option to modestly improve weight and body composition in overweight women.

How similar studies have gone: Some preclinical and small human studies suggest sea buckthorn has antioxidant and lipid‑modulating effects, but rigorous randomized trials showing clear body composition benefits are limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion criteria females, age 18-50, bmi greater or equal to 25. exclusion criteria current pregnancy or lactation, a history of chronic metabolic or gastrointestinal diseases, use of weight management drugs or supplements, known allergies to sea buckthorn or other documented intolerances, smoking or alcohol consumption, a physical activity level exceeding 1.4, and prior participation in weight loss research programs

Where it's running

  • University of veterinary and animal sciences, Lahore
    Lahore, Punjab Province, Pakistan
    Recruiting

Study contacts

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.