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The objective of our study is to investigate whether the use of obstetric gel shortens the first and second stage of labor and exerts a protective effect on the lower genital tract in women undergoing a Vaginal Birth After Cesarean (VBAC).
Recent literature shows that birth injury is associated with postpartum pelvic floor dysfunction (pelvic organ prolapse and fecal and urinary incontinence). Prolonged labor, namely during the 2nd stage, is one of the main obstetric risk factors responsible for anal sphincter rupture and fecal incontinence. In addition, it is associated with increased maternal and neonatal morbidities including increased risk of lower genital tract lacerations. In an effort to shorten labor and decrease lower genital tract trauma many techniques have been investigated.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| obstetric gel group | Experimental | they will have the standard care during labor and delivery with the vaginal application of the obstetrical gel. |
|
| no intervention group | No Intervention | they will receive the standard care during labor and delivery without the use of the obstetrical gel |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| obsteric gel(k-Y jelly) | Drug | A sterile obstetric gel( K-Y Jelly 82GM; manufactured by Johnson& Johnson) will be used for this trial. The obstetric gel is a birth gel with no pharmacologic effects that have purely physical activity. Starting with the first vaginal examination the obstetric gel will be used. After each vaginal examination, 3-5 mL of obstetric gel will be introduced into the vaginal birth canal in the area in front of the child manually or using the sterile obstetric gel applicator without any manipulation or massage. |
| Measure | Description | Time Frame |
|---|---|---|
| length of the second stage of labor | the length of the second stage of labor starting from full cervical dilatation till delivery of the fetus will be recorded. | 1 hour |
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Inclusion Criteria:
• Age between 18 and 40 years
Exclusion Criteria:
• Contraindications for vaginal delivery (placenta previa, active herpes infection, etc…)
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| Name | Affiliation | Role |
|---|---|---|
| AHMED SAMY, MD | Cairo University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Ahmed Ashour | Giza | 12944 | Egypt |
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