CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 20 enrolled
Drug / intervention
Embella (Deoxycholic acid, produced by Espad Pharmed Co.)device
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/NCT06509438
NCT06509438N/ACompleted

Evaluating the Effectiveness and Safety of Embella (Deoxycholic Acid, Produced by Espad Pharmed Co.) for the Management of Submental Fat

Espad Pharmed·interventional·Posted Jul 19, 2024·Updated Sep 19, 2025

In Brief

A clinical study evaluating Embella (Deoxycholic acid, produced by Espad Pharmed Co.) for Submental Fullness. Completed, enrolled 20 participants across 1 site.

Detailed Summary

Submental fat (SMF) is a factor affecting beauty that makes people feel uncomfortable about themselves. In 2015, deoxycholic acid with the brand name KYBELLA® was approved by the American FDA for treatment of submental fat. The purpose of this study is to evaluate the safety and effectiveness of deoxycholic acid injection with the brand name Embella®, manufactured by Espad Pharmed Company, for treatment of this condition. Research Objectives Primary objective: Effectiveness and safety of Embella® in reducing submental fat Secondary objective: Effectiveness assessment of Embella® in improving SMF grading Effectiveness assessment of Embella® in reducing submental fat diameter

Study Details

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

Timeline

N/ACompletedFinished
202420252026
First PostedJul 19, 2024
Enrollment StartApr 10, 2023
Primary CompletionJan 1, 2024
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 2.0 years ago

Interventions

Embella (Deoxycholic acid, produced by Espad Pharmed Co.)device

2 milliliters of Embella injectable solution containing 20 milligrams of deoxycholic acid