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Effectiveness and Safety Evaluation of Embella (Deoxycholic Acid, by Espad Pharmed Co.) in Management of Submental Fat

Not Applicable
Completed
Conditions
Submental Fullness
Interventions
Device: Embella (Deoxycholic acid, produced by Espad Pharmed Co.)
Registration Number
NCT06509438
Lead Sponsor
Espad Pharmed
Brief 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

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Age between 18 and 65 years.
  • Individuals with unwanted submental fat of any severity.
  • Ability to comply with visit schedules and study procedures.
  • Signed informed consent form and agreement to a 3-month follow-up.
Exclusion Criteria
  • Any previous intervention for the treatment of submental fat (SMF).
  • Specific anatomical features or previous damage to the intervention site (e.g., scars, liposuction, swallowing difficulties, enlarged thyroid or lymph nodes) that could interfere with the assessment of intervention outcomes.
  • Evidence of submental enlargment due to reasons other than SMF.
  • History of dysphagia.
  • Body mass index (BMI) > 30 kg/m².
  • Individuals currently on a weight loss program.
  • History of allergy to any components of the drug or local anesthetics.
  • Presence of any inflammation, active infection, unhealed wounds, or skin lesions in the injection area.
  • Use of any anticoagulants, NSAIDs, or any other medications that increase the risk of coagulation disorders within 7 days before injection.
  • Unrealistic expectations.
  • Pregnant or breastfeeding women.
  • Individuals on sodium-restricted diets, such as those with uncontrolled hypertension.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Embella (Deoxycholic acid, produced by Espad Pharmed Co.)Embella (Deoxycholic acid, produced by Espad Pharmed Co.)The intervention included a minimum of one and a maximum of three treatment sessions, of 2 milliliters of Embella (Deoxycholic acid, produced by Espad Pharmed Co.) injectable solution containing 20 milligrams of deoxycholic acid per session, spaced at least 4 weeks apart.
Primary Outcome Measures
NameTimeMethod
A minimum of one grade improvement in the standard submental fat (SMF) assessment gradingweeks 4 and 12 after the last injection

The scales are from 0 to 4, 0 indicating no localized submental fat and 4 indicating extreme submental convexity

Secondary Outcome Measures
NameTimeMethod
Pain intensity was assessed using the VAS from 0 to 10day 1, week 4 and 8

Visual Analogue Scale (VAS): pain intensity scale where 0 indicates no pain and 10 indicates the maximum pain imaginable

Assessment of all adverse events immediately after the injections and during the study period.Immediately after all of the injections and at weeks 4 and 12 after the last injection

Safety assessment including the incidence of all reported AEs and severity graded as follows: mild = 1, moderate = 2, and severe = 3

Measurement of submental fat thicknessWeeks 4 and 12 after the last injection

Using calipers

Subject satisfaction was assessed using the VAS from 0 to 10,week 4 and 12 after the last injection

Visual Analogue Scale (VAS): satisfaction factor scale where 0 indicates complete dissatisfaction and 10 indicates maximum satisfaction

Trial Locations

Locations (1)

Center for Research and Training in Skin Diseases and Leprosy

🇮🇷

Tehran, Iran, Islamic Republic of

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