The Effect of Oral Probiotics on Glycemic Control of Women With Gestational Diabetes Mellitus
Primary Purpose
Gestational Diabetes Mellitus
Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Femina II
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Gestational Diabetes Mellitus
Eligibility Criteria
Inclusion Criteria:
- Pregnant women who were diagnosed with GDM from 13 to 32.6 gestational weeks
- 18 years old and older
- Singleton pregnancy
Exclusion Criteria:
- Women with pre-gestational diabetes mellitus
- GDM diagnosed ≥ 33 gestational weeks
- Women using prophylactic antimicrobial treatment
- Immunocompromised women
- Multiple pregnancy
- Women taking oral probiotic products who refuse to stop the consumption (food-containing probiotics is not considered an exclusion criterion).
Sites / Locations
- Assuta-Ashdod medical center
- Rambam medical center
- Wolfson medical center
- Poriya Medical center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
probiotic femina II
Placebo
Arm Description
research group will receive the probiotic formula Femina II (2 capsules/day) until delivery.
control group will receive a placebo (2 capsules/day) until delivery.
Outcomes
Primary Outcome Measures
The rate of women who will require pharmacotherapy for glycemic control.
Mean value of the mean daily glucose charts after 2 weeks of treatment with the study products.
Secondary Outcome Measures
The rate of women with controlled diabetes
Mean daily glucose charts
Mean daily pre-prandial glucose values
Mean daily post-prandial glucose values
Level of glycated molecules
The rate of women with mean pre-prandial values ≥ 95 mg/dl, mean post-prandial values ≥ 130 mg/dl, and mean daily glucose > 100 mg/dl
The rate of cesarean deliveries
The rate of labor inductions
The rate of birth weight≥4000 gr
The rate of birth weight> 90th percentile
The rate of admission to the neonatal intensive care unit
Apgar score at 1 and 5 minutes from birth
The rate of neonatal hypoglycemia
The rate of neonatal hyperbilirubinemia
The rate of neonatal polycythemia
The rate of neonatal hypocalcemia
The rate of neonatal hypomagnesemia
Cord blood pH levels
The rate of neonatal malformations and developmental disorders
birth weight
Head circumference
Maternal adverse effects
Duration of time until pharmacotherapy for glycemic control is indicated
Full Information
NCT ID
NCT03864549
First Posted
January 21, 2019
Last Updated
August 2, 2021
Sponsor
HaEmek Medical Center, Israel
1. Study Identification
Unique Protocol Identification Number
NCT03864549
Brief Title
The Effect of Oral Probiotics on Glycemic Control of Women With Gestational Diabetes Mellitus
Official Title
The Effect of Oral Probiotics on Glycemic Control of Women With Gestational Diabetes Mellitus - Randomized, Double Blind, Placebo Controlled Trial, Phase 4
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
January 8, 2020 (Actual)
Primary Completion Date
June 1, 2021 (Actual)
Study Completion Date
August 1, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
HaEmek Medical Center, Israel
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Scientific background: Uncontrolled gestational diabetes mellitus (GDM) is associated with severe maternal and neonatal morbidities. Treatment of GDM is multidisciplinary and includes lifestyle changes and medications. However, the efficacy of these treatments is limited due to poor motivation, daily painful blood tests and multiple injections.
Probiotic supplements were shown to modulate the gut microbiome by reducing the adverse metabolic effects associated with pathogenic microbial colonization. Promising effects on glycemic control and insulin resistance in non-pregnant diabetic patients were reported. However, the effect of probiotics on glycemic control in GDM has not been elucidated.
Objectives: To examine the effect of a mixture of probiotic strains given daily on maternal glycemic parameters, and pregnancy outcomes among women with GDM.
Working hypothesis: Oral administration of probiotics will be effective in glucose control of patients with GDM and their neonates without causing significant adverse effects.
Type of research and methods of data collection: A prospective randomized, double blind, placebo controlled trial. Women newly diagnosed with GDM will be recruited and followed in the GDM clinic and Maternal-Fetal Medicine ward (including the research clinic) at Emek Medical Center. They will be divided into a research group, receiving the probiotic formula Femina II and a control group, receiving a placebo (2 capsules/day) until delivery. Glycemic control will be evaluated by daily glucose charts. After 2 weeks of diet and probiotic/placebo treatment and thereafter, pharmacotherapy will be started in case of poor glycemic control according to the daily glucose charts. Blood tests for glycated molecules will be performed. Fetal well-being and growth will be assessed. The primary outcomes are:
The rate of women requiring medications for glycemic control
Mean value of the mean daily glucose charts after 2 weeks of treatment with the study products.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes Mellitus
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
93 (Actual)
8. Arms, Groups, and Interventions
Arm Title
probiotic femina II
Arm Type
Experimental
Arm Description
research group will receive the probiotic formula Femina II (2 capsules/day) until delivery.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
control group will receive a placebo (2 capsules/day) until delivery.
Intervention Type
Dietary Supplement
Intervention Name(s)
Femina II
Intervention Description
2 capsules per day until delivery
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
2 capsules per day until delivery
Primary Outcome Measure Information:
Title
The rate of women who will require pharmacotherapy for glycemic control.
Time Frame
During the length of pregnancy (up to 9 months)
Title
Mean value of the mean daily glucose charts after 2 weeks of treatment with the study products.
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
The rate of women with controlled diabetes
Time Frame
During the length of pregnancy (up to 9 months)
Title
Mean daily glucose charts
Time Frame
During the length of pregnancy (up to 9 months)
Title
Mean daily pre-prandial glucose values
Time Frame
During the length of pregnancy (up to 9 months)
Title
Mean daily post-prandial glucose values
Time Frame
During the length of pregnancy (up to 9 months)
Title
Level of glycated molecules
Time Frame
During the length of pregnancy (up to 9 months)
Title
The rate of women with mean pre-prandial values ≥ 95 mg/dl, mean post-prandial values ≥ 130 mg/dl, and mean daily glucose > 100 mg/dl
Time Frame
During the length of pregnancy (up to 9 months)
Title
The rate of cesarean deliveries
Time Frame
At delivery
Title
The rate of labor inductions
Time Frame
At delivery
Title
The rate of birth weight≥4000 gr
Time Frame
At delivery
Title
The rate of birth weight> 90th percentile
Time Frame
At delivery
Title
The rate of admission to the neonatal intensive care unit
Time Frame
Within a week from delivery
Title
Apgar score at 1 and 5 minutes from birth
Time Frame
Within 1-5 minutes after delivery
Title
The rate of neonatal hypoglycemia
Time Frame
Within 1-2 days after delivery
Title
The rate of neonatal hyperbilirubinemia
Time Frame
Within a week from delivery
Title
The rate of neonatal polycythemia
Time Frame
Within a week from delivery
Title
The rate of neonatal hypocalcemia
Time Frame
Within a week from delivery
Title
The rate of neonatal hypomagnesemia
Time Frame
Within a week from delivery
Title
Cord blood pH levels
Time Frame
At delivery
Title
The rate of neonatal malformations and developmental disorders
Time Frame
1-2 days after delivery
Title
birth weight
Time Frame
At delivery
Title
Head circumference
Time Frame
1-2 days after delivery
Title
Maternal adverse effects
Time Frame
During the length of pregnancy (up to 9 months)
Title
Duration of time until pharmacotherapy for glycemic control is indicated
Time Frame
During the length of pregnancy (up to 9 months)
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Pregnant women who were diagnosed with GDM from 13 to 32.6 gestational weeks
18 years old and older
Singleton pregnancy
Exclusion Criteria:
Women with pre-gestational diabetes mellitus
GDM diagnosed ≥ 33 gestational weeks
Women using prophylactic antimicrobial treatment
Immunocompromised women
Multiple pregnancy
Women taking oral probiotic products who refuse to stop the consumption (food-containing probiotics is not considered an exclusion criterion).
Facility Information:
Facility Name
Assuta-Ashdod medical center
City
Ashdod
Country
Israel
Facility Name
Rambam medical center
City
Haifa
Country
Israel
Facility Name
Wolfson medical center
City
H̱olon
Country
Israel
Facility Name
Poriya Medical center
City
Tiberias
Country
Israel
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32575163
Citation
Okesene-Gafa KA, Moore AE, Jordan V, McCowan L, Crowther CA. Probiotic treatment for women with gestational diabetes to improve maternal and infant health and well-being. Cochrane Database Syst Rev. 2020 Jun 24;6(6):CD012970. doi: 10.1002/14651858.CD012970.pub2.
Results Reference
derived
Learn more about this trial
The Effect of Oral Probiotics on Glycemic Control of Women With Gestational Diabetes Mellitus
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