MedPath

The efficacy and safety of Deoxycholic acid injection in reduction of flank fat

Phase 4
Not yet recruiting
Conditions
Localized adiposity
Flank fat.
Registration Number
IRCT20240416061507N1
Lead Sponsor
Espad Pharmed Co
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
30
Inclusion Criteria

Mild to moderate flank fat (clinically proven and based on caliper measurements and ultrasound criteria)
Ability to complete the study and follow instructions
Informed consent to participate in the study
Consent on not performing any other intervention in the flank area during the study period

Exclusion Criteria

Severe medical or psychological conditions that interfere with the study results
History of hypersensitivity to components of the product under study
Pregnancy and breastfeeding
History of previous flank fat treatment
BMI >??
Patients prone to intravascular volume reduction
Evidence of recent alcohol or drug abuse
History of bleeding disorders or recent consumption (less than 3 weeks) of thrombolytic drugs, anticoagulants, platelet inhibitors orNSAIDs
History of hypertrophic scarring
Infection, inflammation, dermatosis, unhealed wound, cancer or precancerous lesions at the injection site

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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