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The MOVE-trial: monocryl versus vicryl rapide for skin repair of episiotomies: a randomised controlled trial

Suturing of the skin using Monocryl verses suturing of the skin using Vicryl rapide in women with an uncomplicated mediolateral episiotomy after their first delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN29869308
Enrollment
250
Registered
2016-04-20
Start date
2010-11-15
Completion date
Unknown
Last updated
2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Episiotomy Pregnancy and Childbirth Perineal laceration during delivery

Interventions

In both arms the episiotomy was sutured as follows: The vaginal wall was sutured continuously using Vicryl rapide 2-0 from the apex to the hymen. The bulbocavernosus and superficial perineal muscles

Sponsors

Ikazia Hospital, Department of Obstetrics and Gynaecology
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Episiotomy 2. Primiparous 3. Informed consent 4. Suturing occurs on the delivery room 5. Age>18 years

Exclusion criteria

Exclusion criteria: 1. Immune compromised patient 2. Coagulopathy or thrombocytopenia 3. Existence of ruptures other than ipsilateral vaginal wall rupture that require suturing and may cause additional complaints of pain 4. Haemorrhage requiring fast intervention 5. Inadequate understanding of the Dutch language

Design outcomes

Primary

MeasureTime frame
Pain scores as measured by a Visual Analoguous Scale (VAS) when in sitting position at 10 days post partum

Secondary

MeasureTime frame
1. Pain, when walking and supine position, using VAS scores at 6 weeks, 3 months 2. Dyspareunia, using the VAS score, measured after 6 weeks, 3 months 3. Wound infections, measured at 10 days, 6 weeks, 3 months 4. Wound dehiscence 10 days, 6 weeks, 3 months 5. Percentage of patients using analgesics, measured at 24 hours, 10 days, 6 weeks, 3 months 6. Percentage of patients that have suture material removed, measured at 10 days, 6 weeks, 3 months 7. Percentage of patients resuming intercourse, measured at 6 weeks, 3 months

Countries

Netherlands

Contacts

Public ContactRoeland Odijk

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 8, 2026