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Ritgen Maneuver and Birth-Related Perineal Trauma: RCT

The Effect of the Ritgen Maneuver on Perineal Trauma During the Second Stage of Labor: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07713173
Enrollment
122
Registered
2026-07-20
Start date
2025-09-09
Completion date
2026-05-26
Last updated
2026-07-20

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

Conditions

Perineal Trauma, Ritgen Maneuver

Keywords

ritgen maneuver, perineal trauma

Brief summary

Perineal trauma is one of the common complications that may occur during the second stage of labor and can negatively affect women's postpartum recovery and quality of life. The Ritgen maneuver is a hands-on perineal protection technique performed during fetal head delivery to control the birth of the fetal head and potentially reduce perineal injury. However, evidence regarding its effectiveness remains inconsistent. This randomized controlled trial aims to evaluate the effect of the Ritgen maneuver on perineal trauma during the second stage of labor. Pregnant women admitted for vaginal birth will be randomly assigned to either the Ritgen maneuver group or the standard care group. The incidence and degree of perineal trauma, episiotomy, and related maternal outcomes will be compared between groups. The findings of this study are expected to contribute to the evidence base regarding perineal protection techniques during vaginal birth and support the development of clinical practices aimed at reducing birth-related perineal trauma

Interventions

OTHERRitgen maneuver

The Ritgen maneuver was performed during crowning and delivery of the fetal head. One hand was used to control the fetal head while the other supported the perineum to facilitate controlled birth and potentially reduce perineal injury

Standard management of the second stage of labor according to institutional practice without application of the Ritgen maneuver.

Sponsors

Medipol University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Participants were randomly assigned to either a Ritgen maneuver group or a control group receiving routine care during the second stage of labor. Perineal trauma outcomes were compared between groups.

Eligibility

Sex/Gender
FEMALE
Age
20 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women aged 20 years or older. * Gestational age ≥37 weeks. * Singleton pregnancy. * Cephalic (vertex) presentation. * Planned vaginal birth. * No perineal massage during the last 4 weeks of pregnancy. * Not regularly engaged in active sports activity. * Willing to participate and provide informed consent

Exclusion criteria

* Fetal anomaly. * Human papillomavirus (HPV) infection. * Herpes simplex virus (HSV) infection. * Presence of perineal edema. * Vulvar varicosities. * Opioid administration during labor. * Prolonged labor. * Labor dystocia. * Development of fetal distress during labor. * Instrumental vaginal delivery (vacuum, Kiwi, or forceps-assisted delivery)

Design outcomes

Primary

MeasureTime frameDescription
Incidence of Perineal TraumaImmediately after birthThe occurrence of any perineal trauma following vaginal birth, including spontaneous perineal lacerations and episiotomy-related perineal injury.

Secondary

MeasureTime frameDescription
Postpartum Pain ScoreWithin 2 hours after birthMaternal postpartum pain assessed using the Visual Analog Scale (VAS), ranging from 0 (no pain) to 10 (worst imaginable pain)

Countries

Turkey (Türkiye)

Contacts

STUDY_DIRECTORGozde Kugcumen

Medipol University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 21, 2026