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TRIDERM D.S. Crema Normalizzante for Neonatal Hyperseborrhea (Cradle Cap) and Associated Cutaneous Manifestations of Mild-to-Moderate Seborrheic Dermatitis in Children Aged 0 to 3 Years

2026年9月30日 更新者:ICIM International S.r.l.

Prospective, Interventional, Single-Center, Single-Arm Clinical Study to Evaluate the Clinical Improvement of Neonatal Hyperseborrhea ("Cradle Cap"), Including Potential Cutaneous Manifestations Associated With Mild-to-Moderate Seborrheic Dermatitis, and the Cutaneous Tolerability of the Cosmetic Product TRIDERM D.S. Crema Normalizzante.

This clinical study aims to evaluate the effects of using the cosmetic product TRIDERM D.S. Crema Normalizzante in children aged 0 to 3 years with neonatal hyperseborrhea ("cradle cap"), potentially associated with manifestations of mild-to-moderate seborrheic dermatitis. The study will assess whether use of the product is associated with an improvement in the clinical signs of the condition, particularly scaling and erythema, and will evaluate its cutaneous tolerability. Caregiver-perceived improvement, as well as additional dermatological, photographic, and instrumental assessments, will also be considered.

調査の概要

状態

まだ募集していません

詳細な説明

This is a prospective, interventional, single-center, single-arm clinical study conducted at Meyer Children's Hospital IRCCS in Florence, Italy. The study is expected to enroll 20 pediatric participants aged 0 to 3 years.

Neonatal hyperseborrhea, commonly referred to as "cradle cap," is a frequent condition during the first months of life and may also occur in association with manifestations of seborrheic dermatitis. As part of the non-pharmacological topical management of these manifestations, cosmetic products may be used to help improve visible skin signs without exerting a pharmacological action.

TRIDERM D.S. Crema Normalizzante is a cosmetic product intended for use as a cosmetic adjunct in the presence of manifestations associated with seborrheic dermatitis. In this study, the product will be applied according to a regimen consisting of an intensive phase, with two applications per day for 10 days, followed by a maintenance phase, with two applications per day on 3 days per week for the subsequent two weeks. At the end of the product-use period, a follow-up period without product application is planned.

There will be no control group or comparator product. Assessments will be performed longitudinally within each participant by comparing the condition observed at baseline with that observed during product use and at follow-up. The overall duration of participation for each participant will be approximately 52 days. The study is exploratory and preliminary in nature and is intended to generate clinical data to support the scientific documentation and cosmetic claims related to the product.

研究の種類

介入

入学 (推定)

20

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

    • Tuscany
      • Florence、Tuscany、イタリア、50139
        • Meyer Children's Hospital IRCCS
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

1秒~3年 (子)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Age from 0 to 3 years.
  • Good general health.
  • Clinical diagnosis of neonatal hyperseborrhea ("cradle cap"), including possible cutaneous manifestations associated with mild-to-moderate seborrheic dermatitis.
  • No use of keratolytic, anti-inflammatory, or antifungal treatments within the 15 days prior to enrollment.
  • Written informed consent provided by the participant's parent(s) or legal guardian.

Exclusion Criteria:

  • Presence of other concomitant dermatological conditions that, in the Investigator's judgment, may interfere with the clinical assessment of the study.
  • Presence of seborrheic dermatitis of greater severity than that specified in the inclusion criteria.
  • Use of specific topical treatments (keratolytics, corticosteroids, or antifungals) on the affected areas within the 15 days prior to enrollment.
  • Participation in another clinical study within the 30 days prior to enrollment.
  • Known or suspected hypersensitivity to one or more components of the study product.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:TRIDERM D.S. Crema Normalizzante

Participants assigned to this single experimental arm will receive the cosmetic product TRIDERM D.S. Crema Normalizzante. The product will be applied twice daily for 10 days during the intensive phase, followed by a maintenance phase consisting of twice-daily application on 3 days per week for the subsequent two weeks. After completion of the product-use period, participants will undergo a 28-day follow-up period without product application.

TRIDERM D.S. Crema Normalizzante is a topical cosmetic product intended for use as a cosmetic adjunct in the presence of skin manifestations associated with seborrheic dermatitis. The product will be applied to the affected skin areas according to a two-phase regimen: an intensive phase consisting of two applications per day for 10 consecutive days, followed by a maintenance phase consisting of two applications per day on 3 days per week for the subsequent 2 weeks. After completion of the 24-day product-use period, no further product application will be performed during the 28-day follow-up period.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change From Baseline in Investigator's Global Assessment (IGA) Score
時間枠:Baseline, Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)

Clinical improvement will be assessed using the Investigator's Global Assessment (IGA), a 5-point scale ranging from 0 to 4: 0 = absent, 1 = very mild, 2 = mild, 3 = moderate, and 4 = severe. The IGA provides an overall assessment of the intensity and extent of the clinical manifestations, with particular consideration of scaling and erythema. Change in IGA score from baseline (T0) will be assessed at subsequent study visits. A decrease in the IGA score indicates clinical improvement.

Baseline, Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)

二次結果の測定

結果測定
メジャーの説明
時間枠
Change From Baseline in Erythema Score
時間枠:Baseline, Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)

Erythema will be assessed by the Clinical Investigator using a 5-point semiquantitative clinical severity scale ranging from 0 to 4, where 0 indicates absence of erythema, 1 very mild erythema, 2 mild erythema, 3 moderate erythema, and 4 severe erythema. Higher scores indicate greater severity/worse outcome. Change from baseline in erythema score will be evaluated at each post-baseline study time point.

Baseline, Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)
Change From Baseline in Scaling Score
時間枠:Baseline, Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)

Scaling will be assessed by the Clinical Investigator using a 5-point semiquantitative clinical severity scale ranging from 0 to 4, where 0 indicates absence of scaling, 1 very mild scaling, 2 mild scaling, 3 moderate scaling, and 4 severe scaling. Higher scores indicate greater severity/worse outcome. Change from baseline in scaling score will be evaluated at each post-baseline study time point.

Baseline, Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)
Percentage of Participants With at Least a 1-Point Change From Baseline in Investigator's Global Assessment (IGA) Score Toward Lower Severity
時間枠:Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)

Participants will be classified as meeting the clinical response criterion if they have at least a 1-point change from baseline in the Investigator's Global Assessment (IGA) score toward lower severity at a post-baseline study time point. The IGA is assessed by the Clinical Investigator using a 5-point semiquantitative clinical severity scale ranging from 0 to 4, where 0 indicates absence of disease signs, 1 very mild, 2 mild, 3 moderate, and 4 severe. Higher scores indicate greater severity/worse outcome. The percentage of participants meeting this criterion will be calculated at each post-baseline study time point.

Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)
Investigator's Global Assessment of Clinical Improvement Compared With Baseline
時間枠:Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)

The Clinical Investigator will provide an overall assessment of clinical improvement compared with baseline (T0). At each post-baseline assessment, the participant's overall clinical condition will be classified as improved, unchanged, worsened, or not evaluable compared with baseline.

Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)
Number and Percentage of Participants With Local Cutaneous Reactions
時間枠:From baseline through the follow-up visit, 28 days after Day 24 (±3 days)

Local cutaneous reactions will be assessed based on events observed by the Clinical Investigator or reported by the participant's parent or legal guardian during the study. Local cutaneous reactions may include erythema, irritation, pruritus, or other skin reactions at the application site. For each reaction, the description, onset date, duration, intensity, location, relationship to the study product, action taken, and outcome will be recorded in the case report form. The number and percentage of participants with at least one local cutaneous reaction will be summarized.

From baseline through the follow-up visit, 28 days after Day 24 (±3 days)
Caregiver-Reported Responses on the Parent/Legal Guardian Product Evaluation Questionnaire
時間枠:Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)

Caregivers will complete a structured parent/legal guardian product evaluation questionnaire assessing perceived improvement in the participant's cutaneous manifestations, child comfort/tolerability, cosmetic acceptability, product use experience, overall satisfaction, and willingness to purchase or recommend the product. The perceived improvement section includes items assessed using a 5-point agreement scale ranging from 1 to 5, where 1 indicates "not at all agree" and 5 indicates "completely agree"; higher scores indicate a more favorable caregiver-reported perception of improvement. Other questionnaire items use categorical response options and will be summarized descriptively as counts and percentages by response category. No total questionnaire score is planned.

Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)

その他の成果指標

結果測定
メジャーの説明
時間枠
Number and Percentage of Participants by Clinical Investigator's Overall Wood's Lamp Assessment Category Compared With Baseline
時間枠:Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)

Affected skin areas will be assessed by the Clinical Investigator using a Wood's lamp. The assessment will include clinical observation of fluorescence-related findings, such as presence or absence of fluorescence, qualitative changes in fluorescence color or intensity, fluorescence distribution, and estimated extent of the fluorescent area. These observations will be used to assign one overall categorical Wood's lamp assessment compared with baseline at each post-baseline visit. Categories will be: improved, unchanged, worsened, or not evaluable. The number and percentage of participants in each category will be summarized at each post-baseline study time point.

Day 10 (±2 days), Day 24 (±2 days), and 28 days after Day 24 (±3 days)

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年10月1日

一次修了 (推定)

2027年2月1日

研究の完了 (推定)

2027年2月1日

試験登録日

最初に提出

2026年9月15日

QC基準を満たした最初の提出物

2026年9月30日

最初の投稿 (実際)

2026年10月6日

学習記録の更新

投稿された最後の更新 (実際)

2026年10月6日

QC基準を満たした最後の更新が送信されました

2026年9月30日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

Individual participant data (IPD) sharing is not planned for this study. Study results may be disseminated in aggregate form, in accordance with applicable ethical and data protection requirements.

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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