No registrations found.
ID
Source
Health condition
Keywords: pelvic floor muscle, vaginal probe, electromyography;
Trefwoorden: bekkenbodemspieren, vaginale sonde, elektromyografie;
Sponsors and support
Public Higher Medical Professional School in Opole, Poland.
Intervention
Outcome measures
Primary outcome
The electromyographic examination of pelvic floor muscles by means of intravaginal probe.
Secondary outcome
none
Background summary
none
Study objective
1. A higher resting and funtional PFM activity is observed in more distal areas from the introitus of the vagina.
2. A higher resting and funtional PFM activity is observed on the anterior wall of the vagina
Study design
Immediately after all examinations are completed for each patient
Intervention
The main objective is to determine how depth of placement of electrodes its influence on functional and resting bioelectrical activity of PFM. Moreover the probe will be placed in two different ways: toward the anterior or posterior wall of the vagina. A secondary objective is to evaluate the correlation between the activity of PFM, which was measured at various areas of vagina
The target population in this study will be healthy, nulliparous women. Lack of control group.
Participants will need to attend the examination once only. The duration
of the examination will be approximately 30 minutes.
The measurements:
Electromyographic examination of pelvic floor muscles by means of the intravaginal probe OPTIMA 3 (Sugar International, France) with 3 independent, hemispherical electrodes (recording plates).
Measurement of electrical activity of PFM will be assessed in standing position. Prior to measurements, each participant will be instructed how to perform an isolated PFM contraction and take positions used in this study. Resting and functional sEMG activity (in microvolts - µV) will be recorded.
ul. K. Bartla 5,
51-618 Wroclaw
Kuba Ptaszkowski
[default]
Poland
+48 71 784 18 56
qbaans@gmail.com
ul. K. Bartla 5,
51-618 Wroclaw
Kuba Ptaszkowski
[default]
Poland
+48 71 784 18 56
qbaans@gmail.com
Inclusion criteria
1. Subject's consent to participate in the study,
2. Attending physician's consent,
3. Nulliparous, healthy woman,
4. Good general well-being.
Exclusion criteria
1. Contraindications to measurements (infection, menstruation),
2. Lack of subject's consent,
3. Gynecological surgeries
4. Worsening of pain ailments during examination,
5. Urinary incontinence
6. Past or present injuries within the pelvis, hip joint or spine,
7.Past or present the occurrence of pregnancy
8. Congenital and inherited anomalies of the reproductive system.
Design
Recruitment
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 |
---|---|
NTR-new | NL4109 |
NTR-old | NTR4254 |
Other | : none |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |