Comparison of Prevention and Appropiate Obstetric Interventions for Prolonged Second Stage Labor at Term Pregnancies During Vaginal Delivery

Randomized Control Trial for Comparison of Prevention and Appropiate Obstetric Interventions for Prolonged Second Stage Labor at Term Pregnancies During Vaginal Delivery

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04888871

Enrollment

150

Registered

2021-05-17

Start date

2020-02-01

Completion date

2021-05-31

Last updated

2021-05-17

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

Conditions

Complicated Labour/Delivery Livebirth, Obstetric Labor Complications, Vacuum Extraction; Failure, Affecting Fetus or Newborn

Keywords

labor stage, second

Brief summary

Randomized Control Trial for Comparison of Prevention and Appropiate Obstetric Interventions for Prolonged Second Stage Labor at Term Pregnancies During Vaginal Delivery.

Detailed description

This study includes prolonged second stage phase and not prolonged second phase in pregnant women to singletons at the weeks between 37-42. Fetal head level will be at or below the ischial spines in all patients.Patients with fully dilated cervix will be included in the study and the bladder will be emptied completely on the labor table. Patients diagnosed with fetal distress will not be included in the study.Indicated patients will be randomly divided into three groups; one group will be only subjected to a Fundal Pressure (Kristaller Maneuver), second group will only be subjected to Vacuum Extraction and the third group will be subjected to both Fundal Pressure (Kristaller Maneuver) and Vacuum Extraction. Maternal episiotomy needs presence of second and third degree perineal tears, presence of postpartum hemorrhage and need for blood transfusion , cesarean rates and fetal first and fifth minute Apgar score , fetal blood gas parameters, presence of fetal trauma, need for neonatal intensive care will be evaluated among three randomized groups.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 45 Years

Healthy volunteers

Inclusion criteria

* term pregnancy weeks between 37-42, singleton, vertex presentations * prolonged second stage of labor * Fetal head is minimum at the level of ischial spin * maternal incompatibility during/after second stage of labor * complete cervical dilatation

Exclusion criteria

* Fetal distress * Uncomplete cervical dilatation * twin pregnancies or polycyesia * Pregnancy weeks lower than 37weeks * other than vertex presentations * Fetal Anomalies

Design outcomes

Primary

Measure	Time frame
maternal morbidity	3 months

Countries

Turkey (Türkiye)

Outcome results