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Trial · NCT07880093

Registered outcomes16

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBirth Satisfaction Scale-Revised Total ScoreA few hours after birth, before hospital discharge.
Birth satisfaction was assessed using the Turkish version of the 10-item Birth Satisfaction Scale-Revised (BSS-R). Total scores range from 0 to 40, with higher scores indicating greater birth satisfaction. The researcher administered the questionnaire face to face and recorded the mother's responses.
PrimaryLATCH Breastfeeding Assessment ScoreDuring the first breastfeeding session after birth.
Breastfeeding was assessed by the researcher through direct observation using the LATCH tool. Its five items assess latch, audible swallowing, nipple type, maternal comfort, and assistance with positioning. Total scores range from 0 to 10, with higher scores indicating better breastfeeding performance.
PrimaryActive-Phase Labor PainDuring labor, after cervical dilatation exceeded 4 cm and before full dilatation.
Pain was assessed once using a 10-cm visual analog scale, ranging from 0 (no pain) to 10 (the most severe pain). Assessment occurred at cervical dilatation greater than 4 cm. Cervical dilatation at assessment varied among participants.
PrimarySecond-Stage Labor PainDuring the second stage of labor, before the birth of the baby.Pain was assessed once using a 10-cm visual analog scale, ranging from 0 (no pain) to 10 (the most severe pain). The rating was obtained during pushing, before the birth of the baby.
PrimaryThird-Stage Labor PainAfter the birth of the baby and before delivery of the placenta.
Pain was assessed once using a 10-cm visual analog scale, ranging from 0 (no pain) to 10 (the most severe pain). The rating was obtained after the birth of the baby and before delivery of the placenta.
PrimaryFourth-Stage PainThirty minutes after delivery of the placenta.Pain was assessed once using a 10-cm visual analog scale, ranging from 0 (no pain) to 10 (the most severe pain).
PrimaryDuration of the Second Stage of LaborFrom full cervical dilatation to the birth of the baby.Duration in minutes from full cervical dilatation (10 cm) to the birth of the baby.
PrimaryCervical Dilatation at Hospital AdmissionAt the first vaginal examination on admission for labor.Cervical dilatation, measured in centimeters, was recorded from the first vaginal examination at hospital admission for labor.
PrimaryNumber of Vaginal Examinations During LaborFrom admission for labor to the birth of the baby.The total number of vaginal examinations performed during labor was recorded for each participant.
PrimaryUse of Labor InductionDuring the labor and birth admission, before the birth of the baby.Whether labor induction was administered was recorded as a binary outcome (yes/no). Decisions were made by the clinical team providing routine care.
PrimaryUse of Analgesia During LaborDuring labor, before the birth of the baby.Whether analgesia was administered during labor was recorded as a binary outcome (yes/no). Decisions were made by the clinical team providing routine care.
PrimaryNeonatal Birth WeightAt birth, during the initial newborn assessment.Neonatal birth weight was recorded in grams from the routine clinical birth record.
PrimaryOne-Minute Apgar ScoreOne minute after birth.Apgar score recorded during routine newborn assessment. Scores range from 0 to 10, with higher scores indicating better neonatal condition.
PrimaryFive-Minute Apgar ScoreFive minutes after birthApgar score recorded during routine newborn assessment. Scores range from 0 to 10, with higher scores indicating better neonatal condition.
PrimaryTen-Minute Apgar ScoreTen minutes after birth.Apgar score routinely recorded for all newborns at the study hospital. Scores range from 0 to 10, with higher scores indicating better neonatal condition.
PrimaryUntrimmed Placental WeightImmediately after delivery of the placenta.
Placental weight was measured in grams immediately after delivery using the same scale for all participants. The membranes and umbilical cord remained attached; the placenta was not trimmed before weighing.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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