Research with human participants

Overview of medical research in the Netherlands

Urethral support after CS in women with breech presentation at term

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Last updated:

nvt

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Ethical review
Approved WMO
Status
Recruitment stopped
Health condition type
Postpartum and puerperal disorders
Study type
Observational non invasive

ID

NL-OMON33701

Source

ToetsingOnline

Brief title

usac

Condition

  • Postpartum and puerperal disorders

Synonym

pelvic floor (dys)function post partum, urethral (hyper)mobility post partum

Research involving

Human

Sponsors and support

Primary sponsor :
Martini Ziekenhuis
Source(s) of monetary or material Support :
geen

Intervention

Keyword :
(hyper)mobility, (in)continence, delivery, ultrasound

Outcome measures

Primary outcome

nvt

Secondary outcome

nvt

Background summary

nvt

Study objective

nvt

Study design

nvt

Study burden and risks

nvt

Public
Martini Ziekenhuis

postbus 30033
9700 rn groningen
Nederland
Scientific
Martini Ziekenhuis

postbus 30033
9700 rn groningen
Nederland

Listed location countries

Netherlands

Age

Adults (18-64 years)
Elderly (65 years and older)

Inclusion criteria

breech presentation at term
CS

Exclusion criteria

earlier surgical procedures in the internal urogenital tract

Design

Study type :
Observational non invasive
Intervention model
:
Other
Allocation :
Non-randomized controlled trial
Masking :
Open (masking not used)
Control :
Active
Primary purpose :
Basic science

Recruitment

NL
Recruitment status
:
Recruitment stopped
Start date (anticipated) :
Enrollment :
60
Type :
Actual

Approved WMO
Date :
Application type :
First submission
Review commission :
RTPO, Regionale Toetsingscie Patientgebonden Onderzoek (Leeuwarden)

Followed up by the following (possibly more current) registration

No registrations found.

Other (possibly less up-to-date) registrations in this register

No registrations found.

In other registers

Register ID
CCMO NL26241.099.08