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Trattamento conservativo o ricostruzione tra le donne con deiscenza della ferita perineale dopo il travaglio vaginale (HEAL)

22 settembre 2026 aggiornato da: Hanna Jangö, Herlev Hospital

Lesione perineale deiscente dopo travaglio vaginale (GUARIGIONE) - Trattamento conservativo o risuratura

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

Panoramica dello studio

Descrizione dettagliata

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 di studio

Osservativo

Iscrizione (Effettivo)

302

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

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

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

Sì

Sessi ammissibili allo studio

Femmina

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

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.

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Modelli osservazionali: COHORT
  • Prospettive temporali: PROSPECTIVE

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Body image
Lasso di tempo: 9-12 months

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

9-12 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Wound healing
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: One month and 9-12 months

Measured by Modified Oxford scale

One month and 9-12 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

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

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

15 settembre 2023

Completamento primario (Effettivo)

20 agosto 2026

Completamento dello studio (Effettivo)

20 agosto 2026

Date di iscrizione allo studio

Primo inviato

30 agosto 2023

Primo inviato che soddisfa i criteri di controllo qualità

30 agosto 2023

Primo Inserito (Effettivo)

7 settembre 2023

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

25 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

22 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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