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Clinical Analysis of the Influence of Using the Skin Care Products on the Diaper Area in Comparison With Using a Cotton Wool Cloth, Moistened With Clear Water on the Skin Physiology of the Newborns From the 1st Day to the 4th Week of Life

2011年6月21日 更新者:Charite University, Berlin, Germany

Standardized Skin Care Regimen in the Diaper Area: a Prospective, Randomized Clinical Study on Skin Barrier Function and Epidermal IL-1α

Study design:

The purpose of the present study is to analyse of the influence of the application of the skin care products on the diaper area (Factor A) and the application of a cotton wool cloth, moistened with clear water on the diaper area (Faktor B) on the skin barrier function of the newborns during the first four weeks. Additionally, the microbiological colonisation of the skin will be observed. After four weeks all infants in both groups will obtain wet wipe and after 8 weeks a facultative measurement will be performed.

Primary and secondary end points:

In the present study, as a primary end point TEWL on the buttock was chosen, because the significant difference between the infants who were bathed and washed in the previous study was found.

Secondary end points are the TEWL on the other measuring points, pH-value and SCH. Additionally, secondary end points are the D-Squame method and the cytokine measurement with Sebutapes.

Hypotheses:

The intention of the study is to evaluate, whether the using of wet wipe on the diaper area has an influence on the TEWL of the newborns. The following hypotheses are present below:

H0 (Null hypothesis): The TEWL is indistinguishable between infants who get cleaned with wet wipe on the diaper area and infants who get cleaned with a cotton wool cloth, moistened with clear water on the diaper area, i.e.

TEWL clear water is equal TEWL wet wipe against H1 (Alternative hypothesis - bilateral): The TEWL is distinguishable between infants who get cleaned with wet wipe on the diaper area and infants who get cleaned with a cotton wool cloth, moistened with clear water on the diaper area, i.e.

TEWL clear water is not equal TEWL wet wipe

調査の概要

状態

完了

詳細な説明

Method and number of subjects:

Monocenter, prospective, randomized study with two parallel groups. To get reliable results, the number of male and female newborns to be included in this study is 40.

The group of 40 healthy full-term newborn babies will be divided into 2 groups:

Number of groups and subjects Application of skin care products

  1. 01-19 Using of wet wipe during the diaper changes
  2. 20-40 Using a cotton wool cloth, moistened with clear water during the diaper changes. The measurement take place at the Clinical Research Center for Hair and Skin Physiology, at the Department of Dermatology, Campus Charité Mitte and also at the Department of Neonatology Campus Charité Mitte, Charité-Universitätsmedizin Berlin.

Study plan:

Application:

All newborns will obtain a standard skin care, according to division into one of the followings groups: it will be used wet wipe during the diaper changes or a cotton wool cloth moistened with clear water. Additionally, the infants of both groups will be bathed twice a week according to following standard schema. The infant will be submerged in bathtub half filled with water, up to the shoulder.The water temperature should be ca. 370C, pH 7.9-8.2 and the bathing should not require longer than 5 minutes.

Inclusion criteria:

All healthy (i.e. meeting none of the non-inclusion criteria) term newborns are possible candidates for the study. The following criteria must be met for enrollment in the study:

  1. Male and female term newborns from 37 completed weeks of gestation, age ≤ 48 hours
  2. Written informed parental consent

Non-inclusion criteria:

  • Any critically ill term newborn, i.e. septic infants, infants born with serious congenital malformation/defects, asphyxia, hydronephrosis, severe intracranial hemorrhage
  • Newborns with known immunodeficiency
  • Newborns with pre-existing skin disease with eruptions covering more than 50% of body surface i.e. congenital ichthyosis, congenital candidiasis
  • Newborn has relevant skin maceration, which influence the measurements or is communicable i.e. urticaria or herpes
  • Any acutely or chronically ill newborn with temperatures below 35°C or above 40°C
  • Newborn is taking part in another study or is during a term of exclusion of a study.

研究の種類

観察的

入学

44

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

  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

サンプリング方法

確率サンプル

調査対象母集団

group of 40 healthy full-term newborn babies

説明

Inclusion Criteria:

  • All healthy (i.e. meeting none of the non-inclusion criteria) term newborns are possible candidates for the study. The following criteria must be met for enrollment in the study:

    1. Male and female term newborns from 37 completed weeks of gestation, age ≤ 48 hours
    2. Written informed parental consent

Exclusion Criteria:

  • Any critically ill term newborn, i.e. septic infants, infants born with serious congenital malformation/defects, asphyxia, hydronephrosis, severe intracranial hemorrhage

    • Newborns with known immunodeficiency
    • Newborns with pre-existing skin disease with eruptions covering more than 50% of body surface i.e. congenital ichthyosis, congenital candidiasis
    • Newborn has relevant skin maceration, which influence the measurements or is communicable i.e. urticaria or herpes
    • Any acutely or chronically ill newborn with temperatures below 35°C or above 40°C
    • Newborn is taking part in another study or is during a term of exclusion of a study

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

コホートと介入

グループ/コホート
BW= using baby wipes and CW= using cotton wool
wet wipe, cotton wool
Group 1 (BW),(n= 01-19):Using of wet wipe during the diaper changes Group 2 (CW),(n=20-40):Using a cotton wool cloth, moistened with clear water during the diaper changes.

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
TEWL
時間枠:second day of life, 14 day of life and 28 day of life
TEWL= transepidermal waterloss
second day of life, 14 day of life and 28 day of life

二次結果の測定

結果測定
メジャーの説明
時間枠
pH
時間枠:second day of life, 14 day of life and 28 day of life
skin pH
second day of life, 14 day of life and 28 day of life
SCH
時間枠:2nd, 14th and 28th day of life
SCH= stratum corneum hydration
2nd, 14th and 28th day of life
D-Squame
時間枠:2nd, 14th and 28th day of life
D-Squame= special adhesive skin foils
2nd, 14th and 28th day of life
Interleukin-1α
時間枠:2nd, 14th and 28th day of life
Interleukin 1 alpha= cytokine
2nd, 14th and 28th day of life
microbiological colonisation
時間枠:2nd, 14th and 28th day of life
microbiological colonisation of umbilical an buttock region
2nd, 14th and 28th day of life

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。

捜査官

  • 主任研究者:Ulrike Blume-Peytavi, MD, PhD、Department of Dermatology, Charite-Universitätsmedizin, Berlin

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

2007年5月1日

研究の完了

2007年10月1日

試験登録日

最初に提出

2010年5月26日

QC基準を満たした最初の提出物

2010年5月26日

最初の投稿 (見積もり)

2010年5月27日

学習記録の更新

投稿された最後の更新 (見積もり)

2011年6月22日

QC基準を満たした最後の更新が送信されました

2011年6月21日

最終確認日

2007年5月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • CRC/wet wipe

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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