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Prospective Study Comparing Two Classification Systems for Second-degree Vaginal Tears During Spontaneous Childbirth to Assess Their Ability to Predict Postpartum Complications.

Prospective Observational Study Comparing Two Classifications of Second-degree Perineal Tears in Spontaneous Vaginal Births, to Evaluate Their Correlation With Postpartum Clinical Outcomes.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07124676
Acronym
LAC-VAG-2025
Enrollment
482
Registered
2025-08-15
Start date
2025-11-04
Completion date
2028-10-01
Last updated
2026-04-28

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

Conditions

Vaginal Laceration During Delivery

Keywords

vaginal laceration, delivery

Brief summary

The goal of this observational study is to learn whether different classification systems for second-degree perineal tears can predict postpartum complications in women undergoing spontaneous vaginal childbirth. The main questions it aims to answer are: Does the Scandinavian classification better predict postpartum complications such as hemoglobin drop, perineal pain, occult muscle injury, and sexual dysfunction? Does the De Simone classification better correlate with these same postpartum outcomes? Researchers will compare the Scandinavian classification and the De Simone classification to see which system more accurately predicts clinically relevant postpartum complications. Participants will: Undergo standard clinical assessment after spontaneous vaginal delivery with a second-degree perineal tear Have their perineal tear classified using both the Scandinavian and De Simone systems Receive routine postpartum evaluation, including hemoglobin measurement, pain assessment (VAS), and perineal ultrasound Complete follow-up assessment of sexual function using the Female Sexual Function Index (FSFI)

Detailed description

Second-degree perineal tears are heterogeneous injuries involving the perineal muscles without anal sphincter involvement, and their anatomical variability may influence postpartum outcomes. Current standard classifications do not provide detailed subclassification, limiting risk stratification. This prospective, single-center observational study evaluates the prognostic performance of two detailed classification systems: the Scandinavian classification (based on the extent of the perineal body) and the De Simone classification (based on vaginal extension and muscle involvement). Participants are consecutively enrolled following spontaneous vaginal delivery with second-degree tears. Classification is performed during routine postpartum examination by trained clinicians using both systems, with independent assessment to minimize misclassification. Data are collected prospectively and managed in a secure electronic database with predefined validation and consistency checks. Source data verification is performed against clinical records, and variables are standardized through a predefined data dictionary. The statistical approach includes multivariable modeling to assess the association between tear subtypes and clinical outcomes, adjusting for relevant confounders. Model performance will be evaluated using standard calibration and discrimination metrics, with predefined strategies for handling missing data. The study is non-interventional and conducted in accordance with Good Clinical Practice.

Interventions

None listed

Sponsors

University of Campania Luigi Vanvitelli
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Female at birth * Age ≥ 18 years * Spontaneous vaginal delivery * Presence of a spontaneous second-degree perineal tear confirmed on -postpartum examination * Ability and willingness to provide informed consent

Exclusion criteria

* Obstetric or medical conditions preventing spontaneous vaginal delivery * Inability to understand study procedures or complete follow-up assessments

Design outcomes

Primary

MeasureTime frameDescription
hemoglobin reductionwithin 48 hours postpartumsignificant hemoglobin reduction (\>2 g/dL from pre- to post-delivery)
moderate-to-severe perineal painwithin 48 hours postpartumVisual Analog Scale (VAS) ≥ 5; (VAS; range 0-10, where 0 = no pain and 10 = worst imaginable pain); moderate-to-severe pain defined as VAS ≥ 5
pathological Female Sexual Function Index (FSFI) total scorewithin 48 hours after the deliveryFSFI total score modification after vaginal laceration Female Sexual Function Index (FSFI total score; range 2-36, where lower scores indicate worse sexual function and higher scores indicate better function), evaluated as change from baseline

Secondary

MeasureTime frameDescription
occult perineal or vaginal muscle lesionswithin 7 days postpartum for ultrasound assessment; at 3 months postpartum for FSFI evaluation.occult perineal or vaginal muscle lesions on postpartum perineal ultrasound;

Countries

Italy

Contacts

CONTACTMarco La Verde, MD, researcher
marco.laverde@unicampania.it+393389412266

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 29, 2026