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Impact of Thermotherapy During Childbirth on Postpartum Perineal Pain (PERISAFE) (PERISAFE)

Primary Purpose

Pelvic Pain

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Heat therapy
Cryotherapy
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Pelvic Pain focused on measuring perineum, pelvic pain, acute pain, pain management, delivery, obstetric, labor stage, second, analgesia, obstetrical, postnatal care, heat therapy, cryotherapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Primiparous women or multiparous women without history of vaginal birth
  • singleton fetus
  • fetal cephalic presentation
  • ≥37 gestational weeks
  • active labor (cervical dilatation ≥ 6 cm)
  • living fetus
  • major female Exclusion Criteria
  • Abnormal fetal heart rate requiring hastening childbirth
  • Fetal malformation, stillbirth
  • History of female genital mutilation
  • Women not understanding French
  • Women with psychiatric condition
  • Anonymous childbirth
  • Minor female
  • No affiliation to a social security scheme (beneficiary or assignee)

Sites / Locations

  • Louis Mourier HospitalRecruiting
  • Cochin HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

No Intervention

No Intervention

Arm Label

Heat therapy

Cryotherapy

Active second stage usual car

Postpartum usual care

Arm Description

Local perineal heat therapy during active second stage of labor

Local perineal cryotherapy during the immediate postpartum period

Standard obstetrical care and perineal protection during active second stage of labor

Standard immediate (<2 hours) postpartum care

Outcomes

Primary Outcome Measures

Change of perineal pain assessed by the VAS (<H24)
Perineal pain intensity, as a mean of several repeated self-reports measure of perineal pain (each 4 hours) on an 11-point visual analogue scale (VAS) from 0 to 10.

Secondary Outcome Measures

Rate of perineal laceration
1st, 2nd, 3rd and 4th (OASIS) degree perineal lacerations
Rate of episiotomy
episiotomy
Perineal healing assessed by the REEDA scale
Evaluation of perineal healing with the REEDA (redness, oedema, ecchymosis, discharge and approximation of the wound edges) scale: values from 0 to 15, higher scores meaning a worse perineal healing.
Change of perineal pain assessed by the VAS (<H96)
Area under the curve of several repeated self-reports measure of perineal pain on an 11-point visual analogue scale (VAS) from 0 to 10.
Consumptions of pain relief medications
Number and type of pain relief medications consumed: paracetamol, nonsteroidal anti-inflammatory drugs, opioids, nefopam
Pain interference on daily functioning assessed by the BPI-SF
Pain interference on daily functioning assessed by the Brief pain inventory-short form scale (BPI-SF), 7 items from the subscale 23, each item independently scored from 0 to 10, higher score meaning higher pain interference on daily functioning.
Perineal complication
Number of health care appointments (in or outpatient care) for perineal reason (general practitioner, midwife, obstetrician-gynaecologist …)
Childbirth experience assessed by the QACE
Childbirth experience assessed by the Short version of the Questionnaire for Assessing the Childbirth Experience (QACE). Scores for the 13 items range from 1-4 with higher scores indicating a more negative childbirth experience.
Rate of exclusive breastfeeding
Breastfeeding as exclusive mode of infant feeding
Rate of exclusive breastfeeding
Breastfeeding as exclusive mode of infant feeding
Rate of breastfeeding complications
Breastfeeding complications reported by women : breast engorgement, mastitis, breast abscess
Urinary incontinence assessed with the ICIQ-UI SF
Urinary incontinence assessed with the ICIQ - UI SF (International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form). Score ranges from 0 to 21, higher scores indicating higher urinary incontinence.
Anal incontinence assessed with the Wexner Score
Anal incontinence assessed with the Wexner Score. Score ranges from 0 to 20, higher scores indicating higher anal incontinence.
Sexual function assessed with the FSFI
Sexual function assessed by 4 items of the satisfaction et pain subscales of the FSFI (Female Sexual Function Index). Higher score for satisfaction (from 1 to 5) means higher satisfaction. Higher scores for pain items means higher pain (from 1 to 5).
Rate of postpartum depression assessed by the EPDS
Postpartum depression assessed with the Edinburgh postnatal depression scale (EPDS). Score ranges from 0 to 30, higher scores meaning more depressive symptoms. Postpartum depression will be defined by a score greater than 12.

Full Information

First Posted
January 24, 2021
Last Updated
September 26, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Fondation Apicil, PRIDE prize, Laboratoire Guigoz, Département Hopsitalo-universitaire Risques et Grossesse, Université de Paris, Institut National de la Santé Et de la Recherche Médicale, France
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1. Study Identification

Unique Protocol Identification Number
NCT04778631
Brief Title
Impact of Thermotherapy During Childbirth on Postpartum Perineal Pain (PERISAFE)
Acronym
PERISAFE
Official Title
Impact of Thermotherapy During Childbirth on Postpartum Perineal Pain: a Multicenter Factorial Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 16, 2022 (Actual)
Primary Completion Date
April 2023 (Anticipated)
Study Completion Date
June 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Fondation Apicil, PRIDE prize, Laboratoire Guigoz, Département Hopsitalo-universitaire Risques et Grossesse, Université de Paris, Institut National de la Santé Et de la Recherche Médicale, France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Perineal pain is common after vaginal birth. Thermotherapy might be effective to limit postpartum perineal pain, thanks to the effects of local heating or cooling application. This study aims to evaluate the impact of thermotherapy during childbirth on postpartum perineal pain.
Detailed Description
Perineal lesions are common during vaginal delivery: 52% of women giving birth in France experience perineal lesions and 20% an episiotomy. Obstetrical anal sphincter injuries (OASIS) are the most feared due to the risk of anal incontinence, but they concerned a minority of women (0.8%). For most of the women with simple lesions of the perineum, the primary consequence is pain. This moderate to severe perineal pain affects between 40% and 95% of women and peaks in intensity the day after childbirth. This pain might be disabling, impair the mobility, the establishment of breastfeeding, the mother-infant bond, alter the emotional state and overall might affect the quality of life of mothers. Thermotherapy provides a minimally invasive and inexpensive alternative to limit perineal pain in postpartum, thanks to the effects of local heating or cooling application to the perineum : Heat therapy with warm compresses, to protect the perineum during active second stage of labor and reduce the degree of perineal injury : the application promotes vasodilation and extensibility of tissues; Cryotherapy with instant cold pack, to prevent the onset of pain in the immediate postpartum period: the application limits the development of oedema or hematoma. Midwives frequently use thermotherapy with heat or cold. However, these practices cannot be recommended due to a lack of data. Moreover, the potentially synergic effect of consecutive application of heat and cold therapy into the perineum during active second stage of labor and immediate postpartum period has never been evaluated. We hypothesize that thermotherapy during childbirth may reduce postpartum perineal pain.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pelvic Pain
Keywords
perineum, pelvic pain, acute pain, pain management, delivery, obstetric, labor stage, second, analgesia, obstetrical, postnatal care, heat therapy, cryotherapy

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
222 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Heat therapy
Arm Type
Experimental
Arm Description
Local perineal heat therapy during active second stage of labor
Arm Title
Cryotherapy
Arm Type
Experimental
Arm Description
Local perineal cryotherapy during the immediate postpartum period
Arm Title
Active second stage usual car
Arm Type
No Intervention
Arm Description
Standard obstetrical care and perineal protection during active second stage of labor
Arm Title
Postpartum usual care
Arm Type
No Intervention
Arm Description
Standard immediate (<2 hours) postpartum care
Intervention Type
Device
Intervention Name(s)
Heat therapy
Other Intervention Name(s)
Warm compresses
Intervention Description
Application of warm compresses, soaked in hot tap water (between 38° and 44 °C), to the perineum, at each contraction or pushing effort from the start of perineum distension until birth.
Intervention Type
Device
Intervention Name(s)
Cryotherapy
Other Intervention Name(s)
Perineal instant coldpack
Intervention Description
Application of a perineal instant col pack to the perineum, after placental delivery or perineum suturing, for at least 20 minutes.
Primary Outcome Measure Information:
Title
Change of perineal pain assessed by the VAS (<H24)
Description
Perineal pain intensity, as a mean of several repeated self-reports measure of perineal pain (each 4 hours) on an 11-point visual analogue scale (VAS) from 0 to 10.
Time Frame
From 2 to 24 hours after delivery
Secondary Outcome Measure Information:
Title
Rate of perineal laceration
Description
1st, 2nd, 3rd and 4th (OASIS) degree perineal lacerations
Time Frame
2 hours after delivery
Title
Rate of episiotomy
Description
episiotomy
Time Frame
2 hours after delivery
Title
Perineal healing assessed by the REEDA scale
Description
Evaluation of perineal healing with the REEDA (redness, oedema, ecchymosis, discharge and approximation of the wound edges) scale: values from 0 to 15, higher scores meaning a worse perineal healing.
Time Frame
3 days after delivery
Title
Change of perineal pain assessed by the VAS (<H96)
Description
Area under the curve of several repeated self-reports measure of perineal pain on an 11-point visual analogue scale (VAS) from 0 to 10.
Time Frame
From delivery to 3 days after delivery
Title
Consumptions of pain relief medications
Description
Number and type of pain relief medications consumed: paracetamol, nonsteroidal anti-inflammatory drugs, opioids, nefopam
Time Frame
3 days after delivery
Title
Pain interference on daily functioning assessed by the BPI-SF
Description
Pain interference on daily functioning assessed by the Brief pain inventory-short form scale (BPI-SF), 7 items from the subscale 23, each item independently scored from 0 to 10, higher score meaning higher pain interference on daily functioning.
Time Frame
2 months after delivery
Title
Perineal complication
Description
Number of health care appointments (in or outpatient care) for perineal reason (general practitioner, midwife, obstetrician-gynaecologist …)
Time Frame
At two months postpartum
Title
Childbirth experience assessed by the QACE
Description
Childbirth experience assessed by the Short version of the Questionnaire for Assessing the Childbirth Experience (QACE). Scores for the 13 items range from 1-4 with higher scores indicating a more negative childbirth experience.
Time Frame
3 days postpartum
Title
Rate of exclusive breastfeeding
Description
Breastfeeding as exclusive mode of infant feeding
Time Frame
At 3 days after delivery
Title
Rate of exclusive breastfeeding
Description
Breastfeeding as exclusive mode of infant feeding
Time Frame
At 2 months after delivery
Title
Rate of breastfeeding complications
Description
Breastfeeding complications reported by women : breast engorgement, mastitis, breast abscess
Time Frame
At 2 months after delivery
Title
Urinary incontinence assessed with the ICIQ-UI SF
Description
Urinary incontinence assessed with the ICIQ - UI SF (International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form). Score ranges from 0 to 21, higher scores indicating higher urinary incontinence.
Time Frame
At 2 months after delivery
Title
Anal incontinence assessed with the Wexner Score
Description
Anal incontinence assessed with the Wexner Score. Score ranges from 0 to 20, higher scores indicating higher anal incontinence.
Time Frame
At 2 months after delivery
Title
Sexual function assessed with the FSFI
Description
Sexual function assessed by 4 items of the satisfaction et pain subscales of the FSFI (Female Sexual Function Index). Higher score for satisfaction (from 1 to 5) means higher satisfaction. Higher scores for pain items means higher pain (from 1 to 5).
Time Frame
At 2 months after delivery
Title
Rate of postpartum depression assessed by the EPDS
Description
Postpartum depression assessed with the Edinburgh postnatal depression scale (EPDS). Score ranges from 0 to 30, higher scores meaning more depressive symptoms. Postpartum depression will be defined by a score greater than 12.
Time Frame
At 2 months after delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primiparous women or multiparous women without history of vaginal birth singleton fetus fetal cephalic presentation ≥37 gestational weeks active labor (cervical dilatation ≥ 6 cm) living fetus major female Exclusion Criteria Abnormal fetal heart rate requiring hastening childbirth Fetal malformation, stillbirth History of female genital mutilation Women not understanding French Women with psychiatric condition Anonymous childbirth Minor female No affiliation to a social security scheme (beneficiary or assignee)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anne CHANTRY, RM & PhD
Phone
01 42 34 55 80
Email
anne.chantry@inserm.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Charly LARRIEU
Phone
01 58 41 28 99
Email
charly.larrieu@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne CHANTRY, RM & PhD
Organizational Affiliation
Assistance publique - Hôpitaux de Paris / INSERM
Official's Role
Study Director
Facility Information:
Facility Name
Louis Mourier Hospital
City
Colombes
ZIP/Postal Code
92700
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Géraldine MEUNIER, RM & MSc
Phone
01.47.60.63.53
Email
geraldine.meunier@aphp.fr
Facility Name
Cochin Hospital
City
Paris
ZIP/Postal Code
75014
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Clémence LOSCUL, RM & MSc
Email
clemence.loscul@aphp.fr

12. IPD Sharing Statement

Plan to Share IPD
No

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Impact of Thermotherapy During Childbirth on Postpartum Perineal Pain (PERISAFE)

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