CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 30 enrolled
Drug / intervention
Deoxycholic Acid Injectiondevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT07004010
NCT07004010N/ACompleted

Evaluating the Efficacy and Safety of Embella (Deoxycholic Acid, Produced by Espad Pharmed Co.) for the Treatment of Flank Fat

Espad Pharmed·interventional·Posted Jun 4, 2025·Updated Jan 21, 2026

In Brief

A clinical study evaluating Deoxycholic Acid Injection for Flank Fat. Completed, enrolled 30 participants across 1 site.

Detailed Summary

Flank region fat is a factor affecting beauty that makes people feel uncomfortable about themselves. In 2015, deoxycholic acid was approved by the American FDA for treatment of flank fat. The purpose of this study is to evaluate the efficacy and safety of deoxycholic acid injection with the brand name Embella®, manufactured by Espad Pharmed Company, for treatment of this condition. The Primary objective of this study was the proportion of participants with grade 1 or higher ("improved, much improved, very much improved") in investigator-assessed Global Aesthetic Improvement Scale (GAIS) at Week 12 Secondary objective was assessment of other efficacy parameters as well as safety of the product

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsFlank Fat
CountriesIran
Collaborators--

Timeline

N/ACompletedFinished
20252026
First PostedJun 4, 2025
Enrollment StartAug 1, 2024
Primary CompletionDec 30, 2024
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 1.1 years ago

Interventions

Deoxycholic Acid Injectiondevice

The intervention include Deoxycholic acid, SC, 0.15 ml each injection, up to 2-4 ml in each site (2 ml at visit 1 for everyone, and 2 ml at visit 2 unless the patient does not agree)