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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01587378
Other study ID # 2011/1434
Secondary ID 2011-002203-15
Status Completed
Phase N/A
First received
Last updated
Start date October 2012
Est. completion date October 31, 2017

Study information

Verified date February 2019
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall aim of the PregMet 2 Study is to investigate whether metformin prevents late miscarriages and preterm deliveries in PCOS women treated with metformin from first trimester of pregnancy to delivery in a large, randomized, controlled, multi-centre trial setting.

The investigators hypothesis is that metformin compared to placebo treatment from the first trimester to term, reduces the prevalence of late miscarriage (gestational week 13-22) and preterm birth (gestational week < 37) in PCOS women diagnosed according to Rotterdam 2003 consensus criteria, with singleton pregnancy.


Recruitment information / eligibility

Status Completed
Enrollment 489
Est. completion date October 31, 2017
Est. primary completion date October 31, 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Age: 18-45 years

- PCOS diagnosed or reconfirmed according to Rotterdam 2003 criteria, not more than 5 years prior to inclusion

- Mode of conception: Any

- Single, viable fetus, diagnosed by vaginal ultrasound

- Gestational week at inclusion: week 6 + 0 to 12 + 0

- Wash out for metformin: at least 7 days

- Able to communicate fluently in the official language at the study cite or English

Exclusion Criteria:

- Any type of diabetes (except GDM in former pregnancy)

- Known liver disease or ALAT > 100 IU/L

- Known kidney disease or creatinine > 110 µmol/L

- Known alcohol or drug abuse

- Use of drugs interfering with metformin: erytromycin (or other macrolides), cimetidine, anticoagulation therapy

- Unsuitable for participation of other reasons

Study Design


Intervention

Drug:
Metformin
Metformin 500 mg tablets, 1 tablet x 2 daily the first week and then 2 tablets x 2 daily from the second week to delivery
placebo
identical placebo tablets, 1 tablet x 2 daily the first week and then 2 tablets x 2 daily from the second week to delivery

Locations

Country Name City State
Iceland Landspital University Hospital Reykjavik
Norway Sykehuset Ålesund Ålesund
Norway Haukeland University Hospital Bergen
Norway Nordlandssykehuset HF Bodø
Norway Sykehuset Innlandet Brumunddal
Norway Vestre Viken Hospital Trust Drammen
Norway Vestre Viken Ringerike sykehus Honefoss
Norway Sykehuset Telemark Skien
Norway Sentralsykehuset i Vestfold Tønsberg
Norway St Olavs Hospital Trondheim
Sweden Karolinska Universitetssjukhus Stockholm
Sweden Norrlands universitetssjukhus Umeå
Sweden Uppsala University Hospital Uppsala

Sponsors (14)

Lead Sponsor Collaborator
Norwegian University of Science and Technology Alesund Hospital, Haukeland University Hospital, Karolinska University Hospital, Landspitali University Hospital, Nordlandssykehuset HF, Norrlands universitetssjukhus Umeå, St. Olavs Hospital, Sykehuset Innlandet HF, Sykehuset Telemark, The Hospital of Vestfold, Uppsala University Hospital, Vestre Viken Hospital Trust, Vestre Viken Ringerike Sykehus

Countries where clinical trial is conducted

Iceland,  Norway,  Sweden, 

References & Publications (1)

Løvvik TS, Carlsen SM, Salvesen Ø, Steffensen B, Bixo M, Gómez-Real F, Lønnebotn M, Hestvold KV, Zabielska R, Hirschberg AL, Trouva A, Thorarinsdottir S, Hjelle S, Berg AH, Andræ F, Poromaa IS, Mohlin J, Underdal M, Vanky E. Use of metformin to treat preg — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary combined incidence of late miscarriages and preterm births This includes spontaneous births, induced vaginal deliveries and operative deliveries on medical indications. at delivery
Secondary NICU admissions and total number of days in NICU/baby 2 months
Secondary number of patients hospitalized at delivery
Secondary Total number of hospitalization days/ hospitalized participant 2 months
Secondary Prevalence of gestational diabetes up to delivery
Secondary Prevalence of preeclampsia up to delivery
Secondary SNP SNP analysis (genetic analysis) at delivery
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