The goal of this clinical trial is to determine if topical application of compresses soaked in 25% magnesium sulfate on painful perineum after birth is effective to alleviate pain. Researchers will compare this treatment to a placebo, compresses soaked in water. Participants will be invited to use their compresses if needed, for 15 minutes, up to four times a day, during their stay at the hospital after giving birth. They will also have to keep a diary of their usage and of their pain.
Background: Despite the high frequency of perineal trauma in obstetrics, management of perineal care and pain is highly variable, relying on very few studies, if any. Treatment of the perineum with compresses soaked in a magnesium sulfate (Epsom salt) solution has not previously been studied but is routinely used in some hospitals in Quebec, Canada. Objectives: This study aims to determine whether compresses soaked in 25% magnesium sulfate in sterile water can alleviate perineal pain in women immediately after childbirth. Population and intervention: Women who have just given birth vaginally and report perineal or vulvar pain of 3/10 or more will be recruited and randomized into an intervention group receiving the treatment (compresses soaked in 25% magnesium sulfate) or a control group receiving a placebo (compresses soaked in water). Methods: This multi-centric, double-blinded randomized clinical trial will be conducted in four hospitals in the province of Quebec, Canada. The investigators plan to recruit a total of 104 participants. Participants will be instructed to apply the compresses on the vulva and perineum for 15 minutes, four times per day, if needed. They will be asked to score their pain before and after using the compresses for the length of their hospital stay, typically between 24 and 48 hours. Secondary outcomes include analgesic use, incidence of complications, participant satisfaction, opinions on feasibility, and any adverse effects caused by the compresses. Discussion: This randomized controlled trial will assess whether the treatment is more effective in relieving pain than the placebo. The study will also determine the safety and feasibility of this method for routine postnatal care. This study could contribute in the long term to the standardization of evidence-based practices for the management of postpartum perineal pain in Canadian hospitals
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Epsom salt solution in water, 25% concentration
Water
Hôpital de Chicoutimi
Chicoutimi, Quebec, Canada
NOT_YET_RECRUITINGHôpital Brome-Missisquoi-Perkins
Cowansville, Quebec, Canada
NOT_YET_RECRUITINGHôpital Charles Lemoyne
Greenfield Park, Quebec, Canada
RECRUITINGPain reduction on the visual and numerical pain scale after each application
customized visual and numerical pain scale (0-10, 0 being no pain at all and 10 being the worse pain)
Time frame: 24hours to 48 hours (duration of the stay at the hospital)
other analgesic usage, by filling a medication usage journal
It includes usually available analgesics, such as acetaminophen, anti-inflammatories, topical analgesics and ice.
Time frame: 24hours to 48 hours (duration of the stay at the hospital)
Satisfaction, opinions of feasibility through a numerical scale
Participants will have to fill this part of their diary before they leave the hospital.
Time frame: 24hours to 48 hours (duration of the stay at the hospital)
Adverse effects, self declared in a journal
A space in the participant's diary is dedicated for them to declare any benign adverse effects. We don't expect any, since the product is already recognized as safe in literature.
Time frame: 24hours to 48 hours (duration of the stay at the hospital)
Judith Lajeunesse, MD
CONTACT
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Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
90
Hôpital Honoré-Mercier
Saint-Hyacinthe, Quebec, Canada
NOT_YET_RECRUITING