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Comparison of delivery rate and duration of labor in sleeping versus sitting position in women undergoing epidural analgesia

Comparison of delivery rate and duration of second stage of labor in sleeping versus sitting position in nulliparous women undergoing epidural analgesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20121006011020N13
Enrollment
528
Registered
2020-10-28
Start date
2020-08-10
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

Labor. Other complications of spinal and epidural anesthesia during labor and delivery

Interventions

Intervention 1: Intervention group:The first group has a standing position (standing or sitting position) in full cervix dilatation until delivery then gives birth in a lithotomy position. Interventi

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Nulliparous Single pregnancy with cephalic presentation 18-35 years old Term pregnancy( 37-42 weeks of pregnancy)

Exclusion criteria

Exclusion criteria: Drug user Having Chronic Disease Addiction Maternal bleeding

Design outcomes

Primary

MeasureTime frame
The kind of delivery. Timepoint: After delivery. Method of measurement: The observation.;The length of the second stage of labor. Timepoint: Full dilatation to birth. Method of measurement: Clock.;Apgar. Timepoint: 1 and 5 minutes after birth. Method of measurement: Observation.;3 rd and 4 rd laceration. Timepoint: After birth. Method of measurement: Observation.;Mother's satisfaction. Timepoint: After delivery. Method of measurement: Questionnaire.;Pain score. Timepoint: Every 15 minute from full dilatation until delivery. Method of measurement: Visual analog scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Khoshideh

Tehran University of Medical Sciences

khooshide@tums.ac.ir+98 21 7788 0909

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026