- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00972894
Group B Streptococcus (GBS) Polymerase Chain Reaction (PCR) Concordance Study
Prospective Evaluation of a Polymerase Chain Reaction (PCR) Assay (GenExpert DX™) for the Rapid Detection of Recto-vaginal Group B Streptococcus (GBS) Colonisation During Intrapartum Screening
The investigators are comparing three different methods of testing for an infection which is commonly found in women. The infection is caused by a bacterium called Group B Streptococcus. About 10-30% of women carry GBS in the vagina or rectum.
During labour this infection can be passed to the neonate. This can lead to the baby developing a serious infection.
However, research has shown that if antibiotic treatment is given to GBS carrying women during labour most of these infections can be avoided.
A new bedside test known as PCR has been shown to produce a GBS diagnostic result in less than an hour. In clinical trials conducted in the US and France this method has been shown to be more accurate than either prenatal vaginal swabs or risk factor assessment. For this reason, PCR may be helpful in screening and treating GBS positive women in the UK.
In this study the investigators will compare each of the following three methods of diagnosis to a gold standard.
- Prenatal vaginal culture swab (at 35 to 37 weeks gestation)- The US approach.
- Risk factor assessment (at the time of admission for labour)- The UK approach
- The new PCR test (at the time of your labour admission)
The investigators will compare the accuracy of each of these methods with the most accurate method for determining the GBS status during labour. This 'most accurate' method is a highly sensitive swab test which unfortunately takes several days to produce a result. For this reason this test will not tell the investigators whether prophylactic antibiotics may be useful during labour (Receiving them after birth is ineffective).
If PCR is shown to be a more accurate method of identifying GBS positive women this may help to reduce the number of infections in new born infants and as a result may help to save lives.
Studieoversigt
Status
Betingelser
Undersøgelsestype
Tilmelding (Forventet)
Kontakter og lokationer
Studiesteder
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London, Det Forenede Kongerige, W1W 5AH
- The Portland Women ansd Children's Hospital
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London, Det Forenede Kongerige, W1W 5QT
- The Portland Hospital
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Patients will be included in the study if they are;
- 18 years or older
- Pregnant and planned admission to Portland Hospital whether full-term or otherwise.
- Willing and able to give informed consent prenatally.
Exclusion Criteria:
- Scheduled for non vaginal birth
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Simon Bignall, Portland Hospital
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- CTO/08/024
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