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Консервативное лечение или наложение швов у женщин с расхождением раны промежности после вагинальных родов (HEAL)

22 сентября 2026 г. обновлено: Hanna Jangö, Herlev Hospital

Разрыв промежности после вагинальных родов (HEAL) – консервативное лечение или наложение швов

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

Обзор исследования

Подробное описание

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.

Тип исследования

Наблюдательный

Регистрация (Действительный)

302

Контакты и местонахождение

В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.

Места учебы

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

Критерии участия

Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.

Критерии приемлемости

Возраст, подходящий для обучения

18 лет и старше (Взрослый, Пожилой взрослый)

Принимает здоровых добровольцев

Да

Полы, имеющие право на обучение

Женский

Метод выборки

Невероятностная выборка

Исследуемая популяция

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.

Описание

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

Учебный план

В этом разделе представлена ​​подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.

Как устроено исследование?

Детали дизайна

  • Наблюдательные модели: COHORT
  • Временные перспективы: PROSPECTIVE

Когорты и вмешательства

Группа / когорта
Вмешательство/лечение
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.

Что измеряет исследование?

Первичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
Body image
Временное ограничение: 9-12 months

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

9-12 months

Вторичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
Wound healing
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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)
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: 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
Временное ограничение: One month and 9-12 months

Measured by Modified Oxford scale

One month and 9-12 months

Соавторы и исследователи

Здесь вы найдете людей и организации, участвующие в этом исследовании.

Спонсор

Следователи

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

Даты записи исследования

Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.

Изучение основных дат

Начало исследования (Действительный)

15 сентября 2023 г.

Первичное завершение (Действительный)

20 августа 2026 г.

Завершение исследования (Действительный)

20 августа 2026 г.

Даты регистрации исследования

Первый отправленный

30 августа 2023 г.

Впервые представлено, что соответствует критериям контроля качества

30 августа 2023 г.

Первый опубликованный (Действительный)

7 сентября 2023 г.

Обновления учебных записей

Последнее опубликованное обновление (Действительный)

25 сентября 2026 г.

Последнее отправленное обновление, отвечающее критериям контроля качества

22 сентября 2026 г.

Последняя проверка

1 сентября 2026 г.

Дополнительная информация

Термины, связанные с этим исследованием

Планирование данных отдельных участников (IPD)

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НЕ РЕШЕНО

Информация о лекарствах и устройствах, исследовательские документы

Изучает лекарственный продукт, регулируемый FDA США.

Нет

Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.

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Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .

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