NCT07627555

Brief Summary

This study aimed to manage dyslipidemia through Polyunsaturated fatty acids based bar among patients with metabolic syndrome.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 6, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 16, 2025

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

May 30, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

June 4, 2026

Completed
Last Updated

June 4, 2026

Status Verified

May 1, 2026

Enrollment Period

3 months

First QC Date

May 30, 2026

Last Update Submit

May 30, 2026

Conditions

Keywords

lipid profileomega 3 fatty acidsmetabolic syndromecardiovascular diseasespoly unsaturated fatty acids

Outcome Measures

Primary Outcomes (2)

  • Body Mass Index

    BMI is defined as body weight in kilograms divided by height in meters squared (kg/m²). BMI cut-off points are used to assess weight status, categorizing individuals as underweight, normal, overweight or obese. Obesity is further classified into grades 1, 2 and 3.

    60 days

  • Lipid Profile

    Total cholesterol, low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C) and triglycerides levels were measured.

    60 days

Study Arms (2)

Control group T0

PLACEBO COMPARATOR

participants have taken one jelly candy as a mid-morning snack for a duration of 2 months.

Dietary Supplement: Jelly Candy

Experimental group T1

EXPERIMENTAL

participants have taken one PUFA bar as a mid- morning snack for a duration of 2 months.

Dietary Supplement: PUFA Bar

Interventions

Jelly CandyDIETARY_SUPPLEMENT

participants were advised to take one jelly candy as a mid-morning snack for a duration of 2 months.

Control group T0
PUFA BarDIETARY_SUPPLEMENT

Participants were advised to taken one PUFA bar as a mid- morning snack for a duration of 2 months.

Experimental group T1

Eligibility Criteria

Age40 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Metabolic syndrome patient's age 40 to 65 years with BMI (above 25 kg/m 2 ) was major part of this study.
  • Patients having Triglyceride levels range from mild to moderate (150 to 499 mg/dL) are included in the study.
  • Patients having LDL (Low density lipoprotein) range from mild (130-159 mg/dL) to moderate (160-189 mg/dL) are included in the study.
  • Patients having HDL (High-density lipoprotein) range from mild to moderate (60 mg/dL or higher) have been included in the study.

You may not qualify if:

  • Lactating and pregnant women will not be included.
  • Patients who are using any kind of medicine.
  • Any person allergic to nuts.
  • Adults suffering from critical health conditions, including cancer.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Lahore

Lahore, Pakistan

Location

Related Links

MeSH Terms

Conditions

DyslipidemiasMetabolic SyndromeCardiovascular Diseases

Condition Hierarchy (Ancestors)

Lipid Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesInsulin ResistanceHyperinsulinismGlucose Metabolism Disorders

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Head University Institute of Diet and Nutritional Sciences

Study Record Dates

First Submitted

May 30, 2026

First Posted

June 4, 2026

Study Start

February 6, 2025

Primary Completion

May 15, 2025

Study Completion

July 16, 2025

Last Updated

June 4, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will share

Locations