- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07569666
Exososmes in Atrophic Scars Management
Evaluation of Intralesional Exosomes Versus Intralesional Saline in The Treatment of Atrophic Scars: A Randomized Controlled Trial
Lay Summary (Simple Explanation)
Atrophic scars are depressed scars that form when the skin does not heal properly, commonly seen after acne or injuries. These scars can affect appearance and confidence, and current treatments may not always give satisfactory results.
This study aims to evaluate a new treatment using exosomes, which are tiny particles naturally released by cells that help in skin repair and regeneration. Researchers will compare the effect of injecting exosomes directly into scars versus injecting a simple saltwater solution (saline), which serves as a control.
Participants will be randomly assigned to receive either exosome injections or saline injections. Neither the patient nor the evaluator may know which treatment is given, to ensure fair comparison.
The goal is to determine whether exosomes can safely and effectively improve the appearance and texture of atrophic scars.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
- Navn: mona Elradi
- Telefonnummer: +201067070550
- E-mail: monaelradi@medicine.zu.edu.eg
Studiesteder
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Zagazig
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Zagazig, Zagazig, Egypten, 44519
- Rekruttering
- Zagazig University Hospitals
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Kontakt:
- mona Elradi
- Telefonnummer: +201067070550
- E-mail: monaelradi@medicine.zu.edu.eg
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-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
Age >18 years
- Either gender
- Scars of any duration
- Multiple scars at one side or both sides of the face.
- Patients are willing to sign written informed consent statements before beginning treatment.
Exclusion Criteria:
- Pregnant females.
- Patients with one scar.
- Hypersensitivity to any of the used treatments.
- Patient with infection at the site of the scar.
- Patients with unrealistic expectations.
- Patient refusing to sign on the consent.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Placebo komparator: Saltvand
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all patients will receive both, exosomes and saline, each injected into one scar.
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Aktiv komparator: Exosomes
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exosomes are injected within the substance of the scar.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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modified Manchester Scar Scale
Tidsramme: 3 months after 4 biweekly sessions
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Scar appearance was assessed using the Modified Manchester Scar Scale.
The Modified Manchester Scar Scale ranges from 4 to 24, with lower scores indicating better scar appearance and higher scores indicating worse scar appearance
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3 months after 4 biweekly sessions
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Scar thickness measurement in millimetres by Ultrasound examination
Tidsramme: 3 months after 4 biweekly sessions
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Scar characteristics, including scar thickness and echogenicity, will be assessed using high-frequency ultrasound examination.
Scar thickness will be measured in millimeters, and changes from baseline to follow-up will be summarized.
Higher scar thickness values indicate greater scar tissue thickness
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3 months after 4 biweekly sessions
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Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 1125/2-3-2025
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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