Status:

COMPLETED

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

Lead Sponsor:

Taipei Veterans General Hospital, Taiwan

Conditions:

Cesarean Section

Surgical Wound

Eligibility:

FEMALE

18+ years

Brief 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 clini...

Detailed 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 in...

Eligibility Criteria

Inclusion

  • Age over 18, scheduling for a transverse incision cesarean section, and using HERADERM Hydrogel Wound Dressing (Sterile) for wound care at the end of the surgery.
  • Gestational age over 37 weeks on the day of the cesarean section.
  • Body mass index (BMI) less than 35 kg/m² on the day of the cesarean section.
  • Subjects must be able to comply with follow-up wound care visits and subsequent monitoring.

Exclusion

  • Subjects unwilling to sign the consent form or with poor compliance.
  • Currently suffering from severe immune-related skin diseases, such as severe urticaria, generalized eczema, pemphigus, lupus erythematosus, etc.
  • Using medications that affect wound healing (e.g., glucocorticoids, anticoagulants and immunosuppressive drugs).
  • Subjects were deemed unsuitable for participation by investigator, such as uncontrolled infection and conditions that interfere with wound healing.

Key Trial Info

Start Date :

July 29 2024

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

January 31 2025

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT06558240

Start Date

July 29 2024

End Date

January 31 2025

Last Update

April 11 2025

Active Locations (1)

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1

Taipei Veterans General Hospital

Taipei, Taiwan