To Explore the Effectiveness and Feasibility of HERADERM Hydrogel Wound Dressing on Caesarean Section Surgical Site

Last updated: April 8, 2025
Sponsor: Taipei Veterans General Hospital, Taiwan
Overall Status: Completed

Phase

N/A

Condition

Pressure Ulcer

Treatment

HERADERM Hydrogel Wound Dressing (Sterile)

Clinical Study ID

NCT06558240
2024-08-023AC
  • Ages > 18
  • Female

Study Summary

The wound of cesarean section involves multiple layers of tissue and often cause significant postoperative pain. The epidermal wound typically heals within 1 to 2 weeks after surgery. In current clinical practice, advanced wound dressings are commonly used for postoperative wound care. The theory of moist wound healing was first proposed by Winter in 1962, advocating that maintaining a moist environment around the wound can accelerate the healing process.

HERADERM Hydrogel Wound Dressing (Sterile) was approved by the Taiwan FDA in 1999. Although HERADERM Hydrogel Wound Dressing (Sterile) are frequently used clinically for post-cesarean section wound care, there have been no comprehensive reports evaluating the effectiveness and clinical application of the dressings to date. The purpose of this study is to explore the effectiveness and feasibility of HERADERM Hydrogel Wound Dressing on caesarean section surgical site and to provide user experience and clinical data for reference by patients and clinical personnel.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Age over 18, scheduling for a transverse incision cesarean section, and usingHERADERM Hydrogel Wound Dressing (Sterile) for wound care at the end of the surgery.

  2. Gestational age over 37 weeks on the day of the cesarean section.

  3. Body mass index (BMI) less than 35 kg/m² on the day of the cesarean section.

  4. Subjects must be able to comply with follow-up wound care visits and subsequentmonitoring.

Exclusion

Exclusion Criteria:

  1. Subjects unwilling to sign the consent form or with poor compliance.

  2. Currently suffering from severe immune-related skin diseases, such as severeurticaria, generalized eczema, pemphigus, lupus erythematosus, etc.

  3. Using medications that affect wound healing (e.g., glucocorticoids, anticoagulantsand immunosuppressive drugs).

  4. Subjects were deemed unsuitable for participation by investigator, such asuncontrolled infection and conditions that interfere with wound healing.

Study Design

Total Participants: 40
Treatment Group(s): 1
Primary Treatment: HERADERM Hydrogel Wound Dressing (Sterile)
Phase:
Study Start date:
July 29, 2024
Estimated Completion Date:
January 31, 2025

Study Description

In this observational, prospective, single-arm study. We aimed to explore the effectiveness and feasibility of HERADERM Hydrogel Wound Dressing (Sterile) on caesarean section surgical site. Written informed consent are obtained before subjects participate in the study. Eligible subjects will be taken initial wound photos and use experimental dressings for postoperative wound care after closure of caesarean section wound site. To evaluate the clinical applicability of the experimental dressings, wound healing assessments will be conducted by independent study nurse during the postoperative period, hospitalization, and follow-up visits. Information of pain intensity experienced by subjects during dressing removal will be collected. Additionally, satisfaction surveys based on subjects' experiences of wearing and changing the experimental dressings will also be collected during the hospitalization and follow-up visits.

Connect with a study center

  • Taipei Veterans General Hospital

    Taipei City,
    Taiwan

    Site Not Available

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