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Treatment of Scars and Dysfunctions of the Pelvic Floor in Postpartum

Treatment of Scarring and Dysfunction of the Pelvic Floor in Postpartum, Through Physical Therapy or by Medical Recommendations in Consultation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04098965
Acronym
NoRFor
Enrollment
90
Registered
2019-09-23
Start date
2017-07-20
Completion date
2020-07-31
Last updated
2019-09-23

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

Conditions

Pelvic Floor Disorders

Brief summary

Recruitment of patients who have suffered third- and fourth-degree perineal tear during childbirth, and who have given birth at the Hospital Universitario Marqués de Valdecilla (Santander, Spain). They are distributed randomly in two groups an experimental group who apply techniques of physiotherapy and a control group, receiving medical treatment. At the same time is recruited the same number of patients who have not suffered tear and whose birth has been instrumental, dividing into two groups, control and experimental. And the same number of patients who have given birth but have not suffered tear or instrumental delivery, divided also into control group and experimental.

Interventions

OTHERphysician treatment

hygienic-dietary recommendations, Kegel exercises and pain relievers

OTHERPysiotherapy techniques

manual therapy techniques, postural re-education and muscle strengthening

Sponsors

Universidad de León
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 49 Years
Healthy volunteers
No

Inclusion criteria

* Patients who have dysfunctions in the pelvic floor after childbirth * Patients who have given birth at the Hospital Universitario Marqués de Valdecilla * Patients who do not have any medical alteration that does not indicate the treatment

Exclusion criteria

* Patients who do not have pelvic floor dysfunctions after childbirth * Patients who have not given birth at the Hospital Universitario Marqués de Valdecilla * Patients who have any medical changes that counter the treatment

Design outcomes

Primary

MeasureTime frameDescription
change in VAS from the start to the endin the begining, at thirth month, at sixth month and at the finish (one year later)Pain
Change in SF36 from de start to the endin the begining, at thirth month, at sixth month and at the finish (one year later)quality of life sorth form
Change in EPIQ from de start to the endin the begining, at thirth month, at sixth month and at the finish (one year later)Epidemiology of Prolapse and Incontinence Questionnaire
Change in OXFORD from the start to the endin the begining, at thirth month, at sixth month and at the finish (one year later)muscle strength

Countries

Spain

Contacts

Primary ContactM. Pilar Master
pilarvidacoli@hotmail.com+34616965978

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026