Suspended

Milk Volume Production in Mothers of Preterm Infants: Electric Pumping Modalities

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

milk expression with electric pump

Procedure
Who is being recruted

Urogenital Diseases+3

+ Female Urogenital Diseases and Pregnancy Complications

+ Obstetric Labor Complications

From 18 to 60 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Supportive Care Study

Interventional
Study Start: August 2013
See protocol details

Summary

Principal SponsorTel-Aviv Sourasky Medical Center
Last updated: March 29, 2016
Sourced from a government-validated database.Claim as a partner

Study start date: August 1, 2013

Actual date on which the first participant was enrolled.

The study will last for 6 days. Each mother will express breast milk following two designed modalities in a random fashion, for two days each. The two designed modalities are: Complete pumping of one breast (first left) for 15 min, followed by complete pumping of the right breast for 15 min, until the breast is empty. Pumping both breast simultaneously for 15 min. At day one of the study, the mothers will follow the standard pumping modality in practice at our department. In between the two studied procedures at day 4 of the study, the mothers will again follow the standard pumping modality. On each day of the study, in the morning after the first expression of the day, a sample of 2 ml of pumped breastmilk will be taken, and the total volume of the daily expressed milk will be recorded.

Principal SponsorTel-Aviv Sourasky Medical Center
Last updated: March 29, 2016
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 18 to 60 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsObstetric Labor ComplicationsObstetric Labor, PrematurePregnancy ComplicationsPremature Birth

Criteria

1 inclusion criteria required to participate
Mothers of Preterms

1 exclusion criteria prevent from participating
HIV infected mothers

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Each mother follows all 3 electric pump modalities in a randomized order.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Department of Neonatology Tel Aviv Medical Center

Tel Aviv, IsraelOpen Department of Neonatology Tel Aviv Medical Center in Google Maps
SuspendedOne Study Center