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Tratamiento conservador o resutura en mujeres con dehiscencia de la herida perineal después del parto vaginal (HEAL)

22 de septiembre de 2026 actualizado por: Hanna Jangö, Herlev Hospital

Desgarro perineal con dehiscencia después del parto vaginal (HEAL): tratamiento conservador o resutura

The goal of this observational study is to make us more aware of the short and long-term outcomes for women having an uncomplicated healing process after a rupture or birth cut in the perineum after giving birth in relation to a healing process with a dehisced wound treated with conservative management or secondary suturing.

Participants will be asked to do

  • A gynecological examination at one month after birth and 9-12 months after birth.
  • Have a picture taken of the healing process
  • Answer a questionnaire at one month, three months, and 9-12 months after birth

Descripción general del estudio

Descripción detallada

The best way to manage perineal wound dehiscence after childbirth is unknown. Currently, there is no agreed best practice recommendation for managing perineal wound dehiscence due to a lack of evidence comparing conservative management with secondary suturing. Therefore, studies are urgently needed to compare the benefits and risks of both treatments. This study has the potential to significantly impact women´s health for those suffering from perineal wound dehiscence.

The investigators want to include 100 women who have had a primary repair of a second-degree tear or episiotomy with a normal/uncomplicated healing process, 100 women with a second-degree tear or episiotomy identified with a dehisced wound treated with secondary resuturing, and 100 women with a second-degree tear or episiotomy identified with a dehisced wound treated with conservative management.

All women who meet the inclusion criteria are recommended the same treatment and follow-up as currently present as standard care at the four hospitals that the investigators are recruiting from. The study deviates from the standard of care by offering two extra clinical examinations, one questionnaire evaluation without clinical examination, and a follow-up with pictures of the perineal tear healing process.

Tipo de estudio

De observación

Inscripción (Actual)

302

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Herlev, Dinamarca, DK-2730
        • Department of Obstetrics and Gynaecology, Copenhagen University Hospital - Herlev and Gentofte

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Femenino

Método de muestreo

Muestra no probabilística

Población de estudio

We want to include 100 women who have had a primary repair of a second-degree tear or episiotomy with an uncomplicated healing process. They will only be recruited from the Perineal Care Clinics at the Department of Obstetrics and Gynecology at the Copenhagen University Hospital - Herlev. Furthermore, we want to include 100 women with a second-degree tear or episiotomy identified with a dehisced wound treated with secondary resuturing, and 100 women with a second-degree tear or episiotomy identified with a dehisced wound treated with conservative management. They will be recruited from the Perineal Care Clinics at the Department of Obstetrics and Gynecology at the Copenhagen University Hospitals - Rigshospitalet, Herlev Hospital, North Zealand Hospital, and Hvidovre Hospital. The women will come for a clinical examination to assess wound infection and healing 4 - 14 days post-partum.

Descripción

Inclusion Criteria:

  • Women with a vaginal delivery who have had a primary repair of a second-degree perineal tear or episiotomy
  • At least 18 years old
  • Able to understand, read and speak Danish or English
  • Able to give informed consent

Exclusion Criteria:

  • None, first, third- and fourth-degree tear
  • Cesarean Section

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Modelos observacionales: COHORT
  • Perspectivas temporales: PROSPECTIVE

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Normal/uncomplicated healing process

100 women with a second-degree tear or episiotomy primarily sutured after labor: identified with a normal/uncomplicated healing process

A clinical examination is needed to assess the healing process for the three groups. After assessing the healing process, we will take pictures of the tear for documentation.

The participant will answer questions, serving as a baseline questionnaire, when arriving at the clinical examination one month post-partum. At three and 9-12 months post-postpartum, they will receive another questionnaire. The questionnaire will consist of validated questions regarding body image, pain, Urogynecological problems as symptoms of prolapse, urinary and anal incontinence, and questions about sexual problems.

Dehisced wound treated with secondary resuturing

100 women with a second-degree tear or episiotomy: identified with a dehisced wound treated with secondary resuturing

A clinical examination is needed to assess the healing process for the three groups. After assessing the healing process, we will take pictures of the tear for documentation.

The participant will answer questions, serving as a baseline questionnaire, when arriving at the clinical examination one month post-partum. At three and 9-12 months post-postpartum, they will receive another questionnaire. The questionnaire will consist of validated questions regarding body image, pain, Urogynecological problems as symptoms of prolapse, urinary and anal incontinence, and questions about sexual problems.

Dehisced wound treated with conservative management

100 women with a second-degree tear or episiotomy: identified with a dehisced wound treated with conservative management

A clinical examination is needed to assess the healing process for the three groups. After assessing the healing process, we will take pictures of the tear for documentation.

The participant will answer questions, serving as a baseline questionnaire, when arriving at the clinical examination one month post-partum. At three and 9-12 months post-postpartum, they will receive another questionnaire. The questionnaire will consist of validated questions regarding body image, pain, Urogynecological problems as symptoms of prolapse, urinary and anal incontinence, and questions about sexual problems.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Body image
Periodo de tiempo: 9-12 months

Measured by the Body-Image questionnaire FGSIS - Female Genital Self-Image Scale

9-12 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Wound healing
Periodo de tiempo: One month

The proportion of women with healed wounds at one month post-partum assessed by clinical examination and REEDA scale (Redness, Oedema, Ecchymosis, Discharge, Approximation of the wound edges). The REEDA scale contains five criteria each receiving a score between 0 and 3. The total score range from 0 - 15 with lower scores representing better-wound healing

One month
Infection rate
Periodo de tiempo: One month

The proportion of women with an infected wound until one month post-partum assessed by clinical examination and measured by REEDA scale

One month
Resuming sexual intercourse
Periodo de tiempo: One month, three months, and 9-12 months

Measured by the PISQ-12 questionnaire which is a short form of the Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-12)

One month, three months, and 9-12 months
Dyspareunia
Periodo de tiempo: One month, three months, and 9-12months

Measured by the PISQ-12 questionnaire which is a short form of the Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-12)

One month, three months, and 9-12months
Woman´s satisfaction with the aesthetic results of the perineal wound
Periodo de tiempo: One month, three months, and 9-12 months

Self-reported. The woman will be asked if she is satisfied with the aesthetic results of the perineal wound

One month, three months, and 9-12 months
Affected breastfeeding
Periodo de tiempo: One month, three months, and 9-12 months

The woman will be asked whether she is breastfeeding or not

One month, three months, and 9-12 months
Re-admission
Periodo de tiempo: Within one month

The women will be asked whether they have been readmitted to the hospital and why within four weeks p.p.

Within one month
Prolapse
Periodo de tiempo: One month, three months, and 9-12 months

Measured by ICIQ-VS questionnaire which is a short form of the International Consultation on Incontinence Questionnaire - Vaginal Symptoms (ICIQ-VS)

One month, three months, and 9-12 months
Urinary incontinence
Periodo de tiempo: One month, three months, and 9-12 months

Measured by the ICIQ-UI SF questionnaire which is a short form of the International Consultation on Incontinence Questionnaire - Urinary Incontinence Short Form (ICIQ-UI SF)

One month, three months, and 9-12 months
Fecal incontinence
Periodo de tiempo: One month, three months, and 9-12 months

Measured by ICIQ-B questionnaire which is a short form of the International Consultation on Incontinence Questionnaire - Bowel (ICIQ-B)

One month, three months, and 9-12 months
Psychological well-being (maternal anxiety or depression)
Periodo de tiempo: Three months, and 9-12 months

Measured by Edinburgh Postnatal Depression Scale (EPDS). EPDS is a self-assessment questionnaire consisting of ten statements and the respondent is asked about their feelings over the last seven days. The answers are scored from 0-3 which gives an endpoint from 0-30. In Denmark, women are said to have depressive symptoms after delivery if they score 11 or higher

Three months, and 9-12 months
Pain intensity
Periodo de tiempo: One month, three months, and 9-12 months

Self-reported pain intensity measured by Visual Analog Scale (VAS-score). Numeric rating scale from 0-10 (0 = no pain - 10 = pain as bad as can be)

One month, three months, and 9-12 months
Consuming painkillers because of pain due to perineal tear
Periodo de tiempo: One month, three months, and 9-12 months

The participant will be asked whether she is consuming painkillers because of pain due to a perineal tear (Yes/No)

One month, three months, and 9-12 months
Pelvic floor muscle contraction
Periodo de tiempo: One month and 9-12 months

Measured by Modified Oxford scale

One month and 9-12 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Hanna M. Jangö, MD, PhD, Copenhagen University Hospital - Herlev and Gentofte

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

15 de septiembre de 2023

Finalización primaria (Actual)

20 de agosto de 2026

Finalización del estudio (Actual)

20 de agosto de 2026

Fechas de registro del estudio

Enviado por primera vez

30 de agosto de 2023

Primero enviado que cumplió con los criterios de control de calidad

30 de agosto de 2023

Publicado por primera vez (Actual)

7 de septiembre de 2023

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

25 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

22 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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