Sea Buckthorn Aqueous Infusion Impact

NCT07313423 | Recruiting

• 1 other identifier: UVAS2
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 1

Brief Summary

• A total of 60 overweight women (BMI 25-29.9 kg/m²), aged 18-50years, will be enrolled and randomized equally into intervention and control groups. The intervention group will consume a 5 g freshly prepared seabuckthorn aqueous infusion daily for 12 weeks, while controls maintain usual habits without supplementation.
• The seabuckthorn aqueous infusion will be prepared by using 250mL of potable boiled water and then cooled to a lukewarm temperature (around 40-45°C). At this point, 5 g of seabuckthorn powder will be added, stirred thoroughly until fully dispersed, and consumed immediately. The infusion will be freshly prepared once daily and administered in the morning after breakfast. Measurements will be conducted using the InBody 270, a validated bioelectrical impedance analyzer employed in this study to obtain accurate assessments of body weight, body mass index (BMI), waist-hip ratio, and visceral fat levels. The device offers segmental analysis and visceral fat estimation through non-invasive, standardized procedures, ensuring consistency and reliability in longitudinal tracking.

Conditions

Body Compostition

Keywords

sea buckthorn; aqueous infusion; body composition

Outcome Measures

Primary Outcomes (2)

• Body weight

  unit of measurement in kilograms will be measured by weight machine

  12 weeks

• Body mass index

  body mass index will be measured using body mass index calculator

  at the end of intervention (12 week)

Secondary Outcomes (2)

• visceral fat

  at the end of intervention period (12 week)

• waist-hip ratio

  at the end of intervention period ( 12 week)

Study Arms (2)

1

PLACEBO COMPARATOR

The participants in the control group will consume placebo that will match in appearance to the supplement and is used to maintain blinding. Participants will consume freshly prepared sea buckthorn aqueous infusion daily for 12 weeks.

Dietary Supplement: Sea buckthorn aqueous infusion

2

EXPERIMENTAL

Drug (Sea buckthorn aqueous infusion) The participants will consume Sea buckthorn aqueous infusion supplementation daily for 12 weeks. it will be prepared by using 5g sb powder in 250 ml of water.

Dietary Supplement: Sea buckthorn aqueous infusion

Interventions

Sea buckthorn aqueous infusion DIETARY_SUPPLEMENT

Sea buckthorn aqueous infusion prepared by using 5g powder in 250 ml water.

1; 2

Eligibility Criteria

• Age: 18 Years - 50 Years
• Sex: female
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

Sponsors & Collaborators

• University of Veterinary and Animal Sciences, Lahore - Pakistan: lead

Study Sites (1)

University of veterinary and animal sciences, Lahore

Lahore, Punjab Province, 5400, Pakistan

RECRUITING

Central Study Contacts

Eesha Naeem, Post graduate

CONTACT

+923264095787; eeshanaeem22@gamil.com

Dr. Qaisar Raza, Phd

CONTACT

+923002479044; qaisar.raza@uvas.edu.pk

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Assistant professor

Model Details: Participants will be randomly assigned into two groups in a 1: 1 ratio to either the treatment group (sea buckthorn aqueous infusion) or control group (placebo), both groups will be followed concurrently for 12 weeks to assess changes in bmi, body weight, visceral fat and waist-hip ratio.

Study Record Dates

• First Submitted: December 17, 2025
• First Posted: January 2, 2026
• Study Start: January 1, 2026
• Primary Completion: March 30, 2026
• Study Completion: April 15, 2026
• Last Updated: January 2, 2026

Record last verified: 2025-12

Data Sharing

• IPD Sharing: Will not share

Locations

PA (1)