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Enrolling by Invitation

NCT Number: NCT07499752

Study on Fewer Tears (SOFT) - The Effect of Local Anesthesia on the Incidence of Perineal Tears in the First Vaginal Birth

The SOFT study investigates whether local anaesthesia during the second stage of labor decreases the incidence of perineal tears, including sphincter injuries, in women with their first vaginal birth (non-instrumental).

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Key information

Age range

18 year–64 year

Sex eligibility

Female

Study type

Observational

Primary location

Danderyd Hospital

Stockholm, 18288, Sweden

About this study

Introduction Perineal tears are the most common complications of vaginal birth. Severe tears can cause long-term physical and psychological morbidity. Preliminary observations suggest that pudendal block and perineal infiltration with local anaesthesia may relax the pelvic floor muscles, reduce pain, and facilitate a more controlled pushing phase. The SOFT study investigates whether local anaesthesia during the second stage of labor decreases the incidence of perineal tears, including sphincter injuries, in women with their first vaginal birth (non-instrumental).

Materials and Methods Data collection for a prospective observational study is ongoing at Danderyd University Hospital. The study documents perineal protection techniques and the incidence of perineal tears in women with their first vaginal birth (non-instrumental). Findings from this preparatory study will guide the design of a randomized, double-blind, controlled trial to evaluate whether pudendal block and perineal infiltration with mepivacaine or placebo have a protective effect on perineal trauma.

The aim is to include 1,350 participants in this observational study. Midwives complete a case report form indicating the use of manual perineal protection, fetal presentation and position, the duration of the second stage, the detailed degree of perineal tear, pain management during the pushing phase, and the need for local anaesthesia during suturing. The full analysis will evaluate associations among perineal protection techniques, local anaesthesia, and the incidence and severity of perineal tears.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pregnant individuals giving birth.
  • Live fetus/fetuses.
  • Gestational week 34 or more at birth.
  • First vaginal birth, i.e., individuals with prior cesarean section can be included.

Exclusion criteria

  • Intrauterine fetal death or stillbirth.
  • Labor resulting in cesarean section or instrumental delivery.

Treatment and study plan

Perineal protection techniques

Other

Perineal protection techniques used by the midwife during a non-instrumental vaginal birth including wet-warm compresses, verbal guidance, oil/gel, perineal massage, two midwives support, pressure relieving position, manual control of the speed of the head's birth, two-step technique, C-grip or Finnish grip for manual perineal protection, supporting the perineum during the delivery of the shoulders, breathing technique during pushing, water birth, acupuncture.

Primary outcomes

  1. Second-degree perineal injury or worse

    Time frame: Within 24 hours of birth

    Perineal injury after childbirth diagnosed clinically resulting in the diagnostic codes O701, O702, or O703 (i.e. second, third or fourth degree injury).

Secondary outcomes

  1. OASI

    Time frame: Within 24 hours from birth

    Perineal injury affecting the external or internal anal sphincter muscles (third- or fourth-degree tear, O702 or O703).

  2. Episiotomy

    Time frame: Immediately at birth.

    Any incision or cut in the perineum to enlarge the vaginal opening during birth.

Other outcomes

  1. Perineal or vaginal injury of any degree

    Time frame: Within 24 hours from birth

    All types of tears and injuries resulting from and diagnosed at childbirth.

Sponsors and collaborators

Lead sponsor

Karolinska Institutet

Other

Collaborators

  • Danderyd Hospital

Registry information

Acronym: SOFT

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Mar 30, 2026
Registry last updated
Apr 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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