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Clinical Trial Summary

A study in the postpartum period reveals that among women who delivered vaginally and having perineal lesions, between 95 and 100% of them suffer from perineal pain (episiotomy, tears from 1st to 4th degree) to 24 hours of vaginal delivery; and between 60 and 91% 7 days after delivery.

Severe pain that is not taken into account can become chronic pain. It has physical and psychological consequences. It is therefore essential to prevent these risks in young mothers.

The main objective of this study is to assess the efficacy of radiofrequency treatment on perineal pain postpartum, after a vaginal delivery, instrumented or not, in patients with perineal lesions.

A double-blind randomized prospective single-center study will be conducted on patients delivering at Marseille's north hospital.

Women who gave birth to the North hospital site, with perineal lesions (tears, episiotomy) will be invited to enroll in the study.

Patients will be then randomized into two groups, one with radiofrequency treatment, the other without treatment with radiofrequency.

The duration of inclusion is provided over 6 months. Each topic will be followed over a period of 1 month. The total study duration is 7 months.

The expected results are a significant reduction in pain scores during the first days postpartum in women with perineal alteration caused by a vaginal delivery instrumented or not. Also an improvement in the quality of life of patients during the first days.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT03172286
Study type Interventional
Source Assistance Publique Hopitaux De Marseille
Contact Florence Bretelle, MD
Phone +33491964525
Email frlorence.bretelle@ap-hm.fr
Status Recruiting
Phase N/A
Start date April 10, 2017
Completion date December 31, 2018

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05468658 - The Effect of Feng Shui Delivery Room Design on Maternal and Infant Health N/A