Pelvic Girdle Pain Early Postpartum: Underlying Condition and Associated Factors
1 other identifier
observational
105
1 country
1
Brief Summary
Background: Pregnancy-related pelvic girdle pain (PGP) can appear during pregnancy, directly after labour or can be delayed to 3 weeks postpartum. Pain is experienced between the posterior iliac crest and the gluteal fold, particularly in the vicinity of the Sacroiliac joints (SIJ). The pain may radiate in the posterior thigh and can also occur in conjunction with/or separately in the symphysis. The endurance capacity for standing, walking, and sitting is diminished. The diagnosis of PGP can be reached after exclusion of lumbar causes. The pain or functional disturbances in relation to PGP must be reproducible by specific clinical tests. Lack of accurate and early diagnosis of the PGP reasons postpartum may contribute to development of chronic condition, lowering quality of life years after delivery. Objectives: The aim of the project is to evaluate the underlying cause of the severe pelvic girdle pain postpartum (whether it is real PGP or diastasis pubic symphysis) and to assess the differences between females with severe postpartum PGP, mild and moderate PGP and with no PGP in terms of: presence of diastasis pubic symphysis, presence of diastasis recti and linea alba dysfunction, factors associated with labour and maladaptive mental processing (catastrophizing). Materials and methods: Because of low incidence of researched conditions, a case control study will be the study design of choice. The subjects with PGP will be matched with those with no PGP. Subjects' assessment will consist of palpation and ultrasonography evaluation of diastasis recti(inter-recti distance), ultrasonography assesment of pubic symphysis (inter-pubic width) and mental processing (catastrophizing assessed with Pain Catastrophizing Scale) analysis. Factors connected with labour (time from epidural anaesthesia injection to full dilatation and delivery) will be also investigated. Expected results: To the investigators' knowledge, postpartum pelvic girdle pain has not been extensively studied so far. The study will bring information about the possible underlying cause of postpartum PGP: whether it is PGP or diastasis pubic symphysis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2019
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 4, 2019
CompletedFirst Posted
Study publicly available on registry
February 8, 2019
CompletedStudy Start
First participant enrolled
April 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 25, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
February 25, 2021
CompletedMay 14, 2021
May 1, 2021
1.9 years
February 4, 2019
May 11, 2021
Conditions
Outcome Measures
Primary Outcomes (2)
Diastasis Recti: ultrasound measurement of inter-recti distance
measurement of inter-recti distance (ultrasound assessment at the level of umbilicus, 2cm over the umbilicus and 2 cm below)
one time assessment, during the hospital stay, within 1st week postpartum
Pubic symphysis distance
assesment of pubic symphysis distance - presence of diastasis pubic symphysis, distance measured by ultrasound
one time assessment, during the hospital stay, within 1st week postpartum
Secondary Outcomes (4)
Pain Catastrophizing Scale
one time assessment, during the hospital stay, within 1st week postpartum
Epidural anaesthesia
during labour (Time form injection to full cervical dilatation)
Epidural anaesthaesia2
during labour (Time form injection to labour)
Diastasis Recti: inter-recti distance
one time assessment, during the hospital stay, within 1st week postpartum
Study Arms (2)
PGP
Patients in early postpartum period experiencing PGP, confirmed with dedicated functional tests
no PGP
Patients in early postpartum period, with no symptoms and signs of PGP
Eligibility Criteria
Women in early postpartum period (during hospital stay)
You may qualify if:
- Natural labour or vacuum extractor or forceps
- for the study group - pain due to PGP confirmed with dedicated functional tests
- for control group with no pain - no pain due to PGP
- agreement to participate
You may not qualify if:
- diseases that can mimic PGP f.ex. Scheuermann disease, rheumatoid arthritis, Ehler's-Danlos Syndrome, hip dysplasia
- major peri-partum events like internal haemorrhage, pelvic fracture
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Centre of Postgraduate Medical Education
Warsaw, Masovian Voivodeship, 01-004, Poland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 4, 2019
First Posted
February 8, 2019
Study Start
April 1, 2019
Primary Completion
February 25, 2021
Study Completion
February 25, 2021
Last Updated
May 14, 2021
Record last verified: 2021-05