Metformin in Intrahepatic Cholestasis of Pregnancy (METRIC)
Primary Purpose
Intrahepatic Cholestases, Pregnancy Complications
Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Metformin
Ursodeoxycholic Acid
Sponsored by
About this trial
This is an interventional treatment trial for Intrahepatic Cholestases focused on measuring Metformin, Ursodeoxycholic acid, Outcomes
Eligibility Criteria
Inclusion Criteria:
- 20+0 to 40 weeks' gestation on day of randomisation
- Itching with a raised serum bile acid above the upper limit of normal
- Normal anomaly scan at 20 weeks
- Aged 18 years or over
- Able to give written informed consent
- No known pre-existing liver disease
Exclusion Criteria:
- Decision already made for delivery within the next 48 hours
- Known allergy to any component of the ursodeoxycholic acid or metformin tablets
- Patients already on metformin for other conditions
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Metformin arm
Ursodeoxycholic acid
Arm Description
Metformin
Ursodeoxycholic acid
Outcomes
Primary Outcome Measures
Normalisation of maternal serum concentration of bile salts and liver enzymes
Normalisation of Bile acids and liver enzymes - both parameters are the cornerstone for a diagnosis of intrahepatic cholestasis. They have been separated into two outcomes due to to the different laboratory indices of measurement. Results will be aggregated together to report number of patients with abnormal results
Normalisation of maternal serum concentration of liver enzymes
Normalisation of liver enzymes Alanine transaminase Aspartate transaminase Bilirubin (total) Gamma glutamyl transferase Results will be aggregated together to report the number of patients with abnormal liver enzymes
Secondary Outcome Measures
Fetal outcomes
Perinatal death
Fetal outcomes
Preterm delivery
Fetal outcomes
Respiratory distress syndrome
Fetal outcomes
Birth weight (g)
Fetal outcomes
Birth weight percentile
Fetal outcomes
Gestational age at delivery
Full Information
NCT ID
NCT03056274
First Posted
December 22, 2016
Last Updated
July 24, 2018
Sponsor
Epsom and St Helier University Hospitals NHS Trust
Collaborators
King's College Hospital NHS Trust, Medway NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT03056274
Brief Title
Metformin in Intrahepatic Cholestasis of Pregnancy
Acronym
METRIC
Official Title
METformin in Intrahepatic Cholestasis of Pregnancy (METRIC) Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Unknown status
Study Start Date
January 2019 (Anticipated)
Primary Completion Date
June 2019 (Anticipated)
Study Completion Date
September 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Epsom and St Helier University Hospitals NHS Trust
Collaborators
King's College Hospital NHS Trust, Medway NHS Foundation Trust
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a pilot study aimed at comparing the effect of metformin versus ursodeoxycholic acid in women with intrahepatic cholestasis in pregnancy. The study will be conducted in three NHS hospital sites, over an 18 month period.
Detailed Description
Intrahepatic cholestasis is a condition that affects pregnant women. It is characterised by itching, usually in the third trimester of pregnancy and is associated with an increase in the liver enzymes and bile salts. This can be associated with maternal and neonatal morbidity, and rarely perinatal mortality.
The investigators propose to assess and compare the effect of Metformin versus Ursodeoxycholic acid on lowering liver enzymes and bile salts, improving maternal morbidity and improving neonatal outcomes.
This study is a pilot study that will be conducted at 3 NHS hospital sites where patients will randomly assigned to receive either Metformin or Ursodeoxycholic acid. There will be 20 patient in each arm. Recruitment will commence in February 2017 and will run for an 18 month period.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intrahepatic Cholestases, Pregnancy Complications
Keywords
Metformin, Ursodeoxycholic acid, Outcomes
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Metformin arm
Arm Type
Active Comparator
Arm Description
Metformin
Arm Title
Ursodeoxycholic acid
Arm Type
Active Comparator
Arm Description
Ursodeoxycholic acid
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
Glucophage
Intervention Description
Metformin Hydrochloride (HCl) Tablets, is an oral antihyperglycemic drug used in the management of type 2 diabetes
Intervention Type
Drug
Intervention Name(s)
Ursodeoxycholic Acid
Other Intervention Name(s)
Destolit®, Urdox®, Ursofalk®, Ursogal®
Intervention Description
Ursodeoxycholic acid (UDCA) is used to treat gallstones and primary biliary cirrhosis. UDCA is also used to treat obstetric cholestasis (OC), a liver condition that occurs specifically in pregnancy.
Primary Outcome Measure Information:
Title
Normalisation of maternal serum concentration of bile salts and liver enzymes
Description
Normalisation of Bile acids and liver enzymes - both parameters are the cornerstone for a diagnosis of intrahepatic cholestasis. They have been separated into two outcomes due to to the different laboratory indices of measurement. Results will be aggregated together to report number of patients with abnormal results
Time Frame
From date of randomisation to date of delivery assessed up to 26 weeks
Title
Normalisation of maternal serum concentration of liver enzymes
Description
Normalisation of liver enzymes Alanine transaminase Aspartate transaminase Bilirubin (total) Gamma glutamyl transferase Results will be aggregated together to report the number of patients with abnormal liver enzymes
Time Frame
From date of randomisation to date of delivery assessed up to 26 weeks
Secondary Outcome Measure Information:
Title
Fetal outcomes
Description
Perinatal death
Time Frame
From date of randomisation to date of delivery assessed up to 26 weeks
Title
Fetal outcomes
Description
Preterm delivery
Time Frame
From date of randomisation to date of delivery assessed up to 26 weeks
Title
Fetal outcomes
Description
Respiratory distress syndrome
Time Frame
Immediately upon delivery date
Title
Fetal outcomes
Description
Birth weight (g)
Time Frame
Immediately upon delivery date
Title
Fetal outcomes
Description
Birth weight percentile
Time Frame
Immediately upon delivery date
Title
Fetal outcomes
Description
Gestational age at delivery
Time Frame
Immediately upon delivery date
Other Pre-specified Outcome Measures:
Title
Fetal outcomes
Description
Presence of meconium
Time Frame
Immediately upon delivery date
Title
Fetal outcomes
Description
APGAR score at 5 minutes
Time Frame
Immediately upon delivery date
Title
Fetal outcomes
Description
Umbilical arterial pH at birth
Time Frame
Immediately upon delivery date
Title
Maternal outcomes
Description
Symptoms (itch) - assessed by questionnaire at clinic visits
Time Frame
From date of randomisation to date of delivery assessed up to 26 weeks
Title
Maternal outcomes
Description
Maximum dose of medication required
Time Frame
From date of randomisation to date of delivery assessed up to 20 weeks
Title
Maternal outcomes
Description
Gestational diabetes
Time Frame
From date of randomisation to date of delivery assessed up to 20 weeks
Title
Maternal outcomes
Description
Postpartum haemorrhage
Time Frame
From date of randomisation to date of delivery assessed up to 26 weeks
Title
Maternal outcomes
Description
Mode of delivery
Time Frame
From date of randomisation to date of delivery assessed up to 20 weeks
Title
Maternal outcomes
Description
Liver failure
Time Frame
From date of randomisation to date of delivery assessed up to 26 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
20+0 to 40 weeks' gestation on day of randomisation
Itching with a raised serum bile acid above the upper limit of normal
Normal anomaly scan at 20 weeks
Aged 18 years or over
Able to give written informed consent
No known pre-existing liver disease
Exclusion Criteria:
Decision already made for delivery within the next 48 hours
Known allergy to any component of the ursodeoxycholic acid or metformin tablets
Patients already on metformin for other conditions
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hassan Shehata, FRCPI, FRCOG
Phone
01372 735735
Ext
6887
Email
hassan.shehata@esth.nhs.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Amanda Ali, MRCPI, MRCOG
Email
amandaha.ali@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hassan Shehata, FRCPI, FRCOG
Organizational Affiliation
Epsom & St Helier University Trust
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
27824743
Citation
Elfituri A, Ali A, Shehata H. Managing Recurring Obstetric Cholestasis With Metformin. Obstet Gynecol. 2016 Dec;128(6):1320-1323. doi: 10.1097/AOG.0000000000001748.
Results Reference
result
PubMed Identifier
32716060
Citation
Walker KF, Chappell LC, Hague WM, Middleton P, Thornton JG. Pharmacological interventions for treating intrahepatic cholestasis of pregnancy. Cochrane Database Syst Rev. 2020 Jul 27;7(7):CD000493. doi: 10.1002/14651858.CD000493.pub3.
Results Reference
derived
Learn more about this trial
Metformin in Intrahepatic Cholestasis of Pregnancy
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