Development of Products Based on Secretom From Stem Cell Conditioned Medium for Melasma Therapy

ConditionMelasma
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age30-60
SponsorDr.dr.Irma Bernadette, SpKK (K)

About this trial

This research is a clinical study with a single-blind randomized clinical trial design (randomized controlled trial) in RSCM-FKUI

This study aims to Assess the effectiveness and safety of intradermal concentrated secretome injection therapy, triple combination cream, and intradermal tranexamic acid injection in melasma patients, determine the quality of life profile of melasma patients after triple combination cream therapy in melasma therapy, and determine SOD levels in melasma patients.

This research will be attended by 90 research subjects

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Women diagnosed with melasma.

Women without melasma and have areas of skin that are clinically free of lesions for SP control.

30-60 years old.

Fitzpatrick skin type IV-V.

Disqualifiers

Pregnant and breastfeeding women.

Currently using hormonal contraception or have ever used contraception hormones in the last 6 months.

Using topical therapy for melasma, for example corticosteroids, tretinoin, hydroquinone, and other therapies that whiten or brighten the skin in the last 2 weeks.

Using topical triple combination cream therapy for at least 3 months and did not show significant improvement

Trial design

Design model

Parallel

Treatments tested in this trial

  • Concentrated secretome Injection 2mL

    Drug

    The secretome used in this research comes from mesenchymal stem cells from adipose tissue produced by IPT RSCM Stem Cell Medical Technology. The secretome produced by mesenchymal stem cells is collected, centrifuged to separate it from debris, and followed by filtration with a 0.22 μm pore filter to ensure sterility. Next, the concentration process is carried out using tangential flow filtration with the Spin-X UF 500® concentrator, packaged, and stored at -80 degrees Celsius. The product used is a sterile product, which is tested for sterility and total protein content. When it is to be used, the secretome is removed from the freezer, warmed (thawing), and injected into the patient according to a predetermined method.

  • Tranexamic acid injection

    Drug

    1. Tranexamic acid 25 mg/ml is prepared by taking tranexamic acid in a vial 250 mg/5 ml as much as 0.5 ml (25 mg) using a 1 ml syringe and diluted with 0.5 ml 0.9% NaCl solution just before being injected into the SP. 2. Tranexamic acid 10 mg/ml is prepared by taking 0.2 ml (10 mg) of AT in a 250 mg/5 ml vial using a 1 ml syringe and diluting it with 0.8 ml of 0.9% NaCl solution for a moment. before injection into the Subject 2\. Tranexamic acid 10 mg/ml is prepared by taking 0.2 ml (10 mg) of AT in a 250 mg/5 ml vial using a 1 ml syringe and diluting it with 0.9% normal saline (NS) 0.8 ml just before injection into the Subject

  • Triple Combination Cream

    Drug

    1. Apply sunscreen SPF ≥30 in the morning on 2 knuckles 2. Apply triple combination cream (Refaquin) containing hydroquinone 40 mg, tretinoin 0.5 mg, and fluocinolone acetonide 0.1 mg at night all over the face except the area around the eyes, 1 fingertip unit (FTU) or 1 knuckle.

Treatment groups

90 Participants
are divided into 3 treatment groups
Group A: Group A (Secretom group)Experimental treatment 1 intervention
Group B: Group B (Triple Combination Group)Experimental treatment 1 intervention
Group C: Group C (Tranexamic Acid Group)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change of Melasma Severity based on modified Melasma Severity Index (mMASI) score.

The range of values for mMASI is between 0 and 24 which can then be divided into mild melasma (0-8), moderate (8-16), and severe (16-24). improvement occurs if the mMASI score decreases by \<50% from the previous visit worsening if score persists or mMASI Score Increase \>50%

Time frame
re-evaluation on day 14, 28, 42, 56 and day 84 of therapy
2

Change of Melasma Severity based on Patient's Tolerability Assesment (PtGA).

one method of evaluating the response to therapy in melasma which is assessed subjectively by the patient. The response to therapy can be assessed as follows No or slight response: \< 25% improvement Moderate response: 25% - 50% improvement Good response: 50% improvement - \< 75% Excellent response: improvement \> 75% The response is said to be good if the score is above 50% since the previous visit

Time frame
re-evaluation on day 14, 28, 42, 56 and day 84 of therapy
3

Change of Melasma Severity based on Dermoscopy

based on Dermoscopy Telangiectasis score assessment using a 5-point dermoscopy-scale: 0 = No visible capillaries. 1 = Elongated capillaries accompanied by dilation, not visible to the naked eye. 2 = Moderate telangiectasis that is beginning to be visible to the naked eye. 3 = Severe telangiectasis characterized by reduced capillary loops. 4 = Very severe telangiectasis characterized by dilatation and loss of capillary loops.

Time frame
re-evaluation on day 84 of therapy
4

Change of Melasma Severity based on Wood's Lamp

Epidermal Type/ Dermal Typed/ Mixed Typed

Time frame
re-evaluation on day 84 of therapy

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Dr.dr.Irma Bernadette, SpKK (K)

Lead sponsor

Indonesia University

Sponsor institution