Examination of intrapartal use of lubricants to shorten birth duration and reduce birth-associated injury, operative vaginal delivery and secondary caesarean sections.
Not Applicable
Recruiting
- Conditions
- P15.5O70.0O70.1O70.2O70.3O71.9O81O82P22.9P21.9
- Registration Number
- DRKS00024599
- Lead Sponsor
- Charité - Universitätsmedizin Berlin Campus Virchow-Klinikum (CVK) & Campus Mitte (CCM) Klinik für Geburtsmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 300
Inclusion Criteria
Nullipara
- 18 - 45 years old
- vital singleton pregnancy
- Gestational age >37+0 weeks
- vaginal birth from skull-position
- fetal estimated weight 2000g - 5000g
- at least twice lubricant application (20ml)
- max. 50ml lubricant per birth
Exclusion Criteria
- Age under 18 years
- Persons who are not able to give their consent
- Multiple pregnancy
- gestational age <37+0 weeks
- Intrauterine death
- vaginal birth from breech-position
- fetal estimated weight <2000g or >5000g
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method