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The length of the second stage of labor in manual rotation at persistent occiput posterior

The effect of manual rotation at persistent occiput posterior on the length of the second stage of labor: a controlled randomized trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110524006582N35
Enrollment
46
Registered
2022-07-27
Start date
2022-06-22
Completion date
Unknown
Last updated
2022-08-29

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

Conditions

The effect of stable posterior occipital manual rotation on the duration of the second stage of labor.

Interventions

Intervention 1: Intervention group: The head of fetus will have rotated manually by a skilled and experienced operator during contraction in full dilatation and effacement of cervix with head statio

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: full term first and second pregnancy singleton second stage of labor (complete dilatation and effusion) Diagnosis of stable occiput by TV and ultrasound confirmation Absence of cardiopulmonary diseases in the mother Absence of congenital problems diagnosed in the fetus (microcephaly, hydrocephalus, encephalitis, etc.) Absence of IUGR No abnormalities in the fetal heart monitor Station between minus one to +3

Exclusion criteria

Exclusion criteria: Have a history of cesarean section or surgery contrary to normal delivery in the vaginal perineum Having a history of infertility

Design outcomes

Primary

MeasureTime frame
Comparison of the length of the second stage of labor in the intervention and control groups. Timepoint: the length of the second stage of labor. Method of measurement: partograph.

Secondary

MeasureTime frame
Comparison of maternal outcomes in intervention and control groups. Timepoint: post-partum. Method of measurement: maternal outcomes checklist.;Comparison of neonatal outcomes between two control intervention groups. Timepoint: immediately after birth, five minutes after birth till 24 hours after birth. Method of measurement: Neonatal Outcomes Checklist and Apgar Table and Fetal Heart Monitoring Checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmahin kamalifard

Tabriz University of Medical Sciences

kamalifardm@tbzmed.ac.ir+98 41 3479 6770

Outcome results

None listed

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