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NCT01417260 · ClinicalTrials.gov registry record

Effects of Breast Feeding on Post-Cesarean and Post-Vaginal Delivery Pain

A clinical trial, sponsored by Stanford University.

Completed
Registry status
130
Enrollment target

NCT01417260: Completed study, sponsored by Stanford University.

NCT01417260 is a clinical trial that has completed, run by Stanford University. The registered enrollment target is 130 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01417260 has completed, sponsored by Stanford University.

COMPLETED
Registry status
130 participants
Enrollment target

Study Summary

Oxytocin is a hormone that is released in response to distension of the cervix and uterus during labor, and after breast feeding as a result of nipple stimulation. In addition to oxytocin facilitating birth and breastfeeding, oxytocin has a number of effects on maternal behavior including bonding, social recognition, anxiolysis, sexual arousal. The role of oxytocin in pain modulation has recently been highlighted. Intranasal or intrathecal (spinal) administration has been found to impact pain modulation. The administration of intravenous oxytocin has not provided effective analgesia because oxytocin is unable to pass to your brain. The role of breastfeeding on analgesia is poorly investigated, which is why we are carrying out this study.

Primary Outcome

The primary outcome measure will be change in pain scores (0=no pain, 10=worse pain imaginable) during and after breastfeeding compared to pain before. We will examine both vaginal, cramping and surgical pain as appropriate. The patients will be given a breastfeeding diary to complete, which will record the average pain scores (0-10) before, during and after each breastfeed.

Trial Details

FieldValue
Enrollment Target 130 participants
Start Date 2011-08
Est. Completion 2014-12
Stanford University

1,744 total trials

What the finished NCT01417260 record still lists

NCT01417260 is an observational study that tracks outcomes without assigning an intervention. The registered 130 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 0 interventions.

NCT01417260 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01417260 about?

NCT01417260 is a clinical study titled "Effects of Breast Feeding on Post-Cesarean and Post-Vaginal Delivery Pain". Oxytocin is a hormone that is released in response to distension of the cervix and uterus during labor, and after breast feeding as a result of nipple stimulation. In addition to oxytocin facilitating birth and breastfeeding, oxytocin has a number of effects on maternal behavior including bonding, s...

What is the current status of trial NCT01417260?

This trial is currently completed. The enrollment target is 130 participants. The study started on 2011-08. Estimated completion is 2014-12.

Who is sponsoring clinical trial NCT01417260?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01417260, the US trial registry maintained by the National Library of Medicine. NCT01417260 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.