Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

A Trial of Sublingual Misoprostol to Reduce Primary Postpartum Haemorrhage After Vaginal Delivery

1. mars 2022 oppdatert av: Dr. Diana Man-Ka Chan, The University of Hong Kong

A Randomized Controlled Trial of Sublingual Misoprostol in Addition to Routine Uterotonics to Reduce Primary Postpartum Haemorrhage in Low Risk Women After Vaginal Delivery

The objective of the randomized controlled study is to compare combination of sublingual misoprostol and routine uterotonics versus routine uterotonics alone on PPH in low risk women after vaginal delivery. The hypothesis is that combination of sublingual misoprostol and routine uterotonics is more effective than routine uterotonics alone in reduction of PPH in low risk women after vaginal delivery.

Studieoversikt

Status

Har ikke rekruttert ennå

Intervensjon / Behandling

Detaljert beskrivelse

The investigators propose a multi-center randomized controlled trial. All women eligible for the trial will be recruited at antenatal clinic or antenatal ward. Women with risk factors for PPH and who are planning for Caesarean delivery will be excluded. Women are informed of the study in the antenatal clinic between 36 to 40 weeks gestation. An information sheet will be distributed and a written consent will be obtained. This trial will involve three maternity units in Hospital Authority (Queen Mary Hospital, Queen Elizabeth Hospital and Pamela Youde Nethersole Eastern Hospital) with total annual delivery of 11673 in 2018. Among the annual delivery of 11000, 70% would be vaginal delivery and 60% of women with vaginal delivery would be at low risk for PPH, about 4600 women per year will be eligible in the three units. The investigators aim to recruit 400-500 women per year in total in the three units and the sample size is 1300 women in total over three years.

Eligible women will be randomly assigned in a 1:1 ratio by a computer-generated list to misoprostol or control group when the women are in active labour. Women in misoprostol group will receive sublingual misoprostol 600 micrograms in addition to routine uterotonics, whereas women in control group will receive routine uterotonics. Central randomization will be performed, generated by stratified block randomization, stratified by individual centers. Randomization will be performed when women are in advanced labour i.e. cervical dilatation at 8cm or more and will be stratified by centres and parity (nulliparous vs multiparous).

Antenatal and intrapartum care of the women will follow routine care. A blood sample for complete blood count will be taken when women are admitted in labour. Active management of third stage of labour will be provided as routine postpartum care (including use of routine uterotonics and controlled cord traction). Delayed cord clamping is allowed at discretion of managing clinicians. Studies have shown the delayed cord clamping is beneficial to newborn and it does not increase risk of maternal bleeding. At delivery of baby, routine uterotonics (syntometrine 1ml intramuscular or syntocinon 5 units intravenous bolus followed by 40 units in 500ml normal saline infusion over 4 hours in women contraindicated for syntometrine) will be given as routine practice, and sublingual misoprostol will be given to women in misoprostol group.

Blood loss will be measured during vaginal delivery by direct collection of blood with a calibrated obstetric drape. The calibrated under-buttock drape folds out into a 1x1 meter sterile surface for delivery. The device allows for blood to be collected into a transparent calibrated pouch with capacity up to 2500ml. There are markings on the pouch that aid blood volume measurement. Immediately after delivery of baby and before delivery of placenta, amniotic fluid will be drained and a surgical drape with a graduated bag will be placed under women's buttock to collect the blood loss. The bag will remain in place for at least 15 minutes and until the birth attendants consider that the bleeding has stopped. Swabs and drapes soaked with blood will be weighed using a standardized scale for blood loss calculation (subtracting the known dry weight of the drapes and swabs) in addition to that collected in the graduated bag. Clinicians who assess the blood loss will be blinded to study group allocation. Maternal blood pressure, pulse and temperature will be recorded every 4 hours for one day after delivery. An observation form will be used to record maternal side effects. Blood will be checked for complete blood count on day 2 after delivery.

In order to standardize various study procedures, training will be provided at individual study sites by investigators. Training will include recruitment procedure, randomization , administration of study drug and blood loss measurement method. Research assistant will have regular visit in various study sites to check consistency of the above procedures.

Investigators will have regular communication and meetings with co-investigators at the study sites to review study procedures and to review study progress and address potential problems arising from the study.

Studietype

Intervensjonell

Registrering (Forventet)

1300

Fase

  • Fase 4

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

  • Navn: Diana Man Ka Chan, MBBS
  • Telefonnummer: (852) 2255 4517
  • E-post: dcmanka@gmail.com

Studer Kontakt Backup

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Hunn

Beskrivelse

Inclusion Criteria:

  • All women age ≥ 18 years (age of legal consent)
  • Singleton pregnancy >= 34 weeks

Exclusion Criteria:

  • Women planning for Caesarean section
  • Women with known risk factors for PPH, including grand multiparity (>=4), multiple pregnancy, fibroid with size >4cm, history of PPH, placenta previa, large-for-gestational age fetus (defined as EFW >90th centile), polyhydramnios, and previous Caesarean section.
  • Women with bleeding tendency or thrombocytopenia < 100 x 109/L
  • Women on anticoagulant or aspirin
  • Women in whom use of misoprostol / syntocinon / syntometrine is contraindicated
  • Women with known hypersensitivity to misoprostol / syntocinon / syntometrine

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Misoprostol group
At delivery of baby, routine uterotonics (syntometrine 1ml intramuscular or syntocinon 5 units intravenous bolus followed by 40 units in 500ml normal saline infusion over 4 hours in women contraindicated for syntometrine) will be given as routine practice, and sublingual misoprostol will be given to women in misoprostol group.
sublingual misoprostol 600 micrograms in addition routine uterotonics at third stage of labour
Andre navn:
  • cytotec
Ingen inngripen: Control group
At delivery of baby, routine uterotonics (syntometrine 1ml intramuscular or syntocinon 5 units intravenous bolus followed by 40 units in 500ml normal saline infusion over 4 hours in women contraindicated for syntometrine) will be given as routine practice, and no additional sublingual misoprostol will be given to women in control group.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Percentage of primary postpartum haemorrhage
Tidsramme: within first 24 hours after delivery
blood loss 500ml or more at delivery
within first 24 hours after delivery

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Percentage of severe postpartum haemorrhage
Tidsramme: within first 24 hours after delivery
blood loss 1000ml or more
within first 24 hours after delivery
Percentage of need for additional uterotonics for treatment of postpartum haemorrhage
Tidsramme: within first 24 hours after delivery
including additional use of syntometrine, syntocinon, carboprost and misoprostol
within first 24 hours after delivery
Duration of third stage of labour
Tidsramme: within first 24 hours after delivery
Time interval between delivery of baby and delivery of placenta
within first 24 hours after delivery
Percentage of need for manual removal of placenta
Tidsramme: within first 24 hours after delivery
Need for manual removal of placenta due to retained placenta
within first 24 hours after delivery
Incidence of uterine atony
Tidsramme: within first 24 hours after delivery
incidence of uterine atony
within first 24 hours after delivery
Change in haemoglobin level (g/dL) after delivery
Tidsramme: within 7 days after delivery
compared with pre-delivery haemoglobin
within 7 days after delivery
Change in haematocrit level (L/L) after delivery
Tidsramme: within 7 days after delivery
compared with pre-delivery haematocrit level
within 7 days after delivery
Percentage for need for blood transfusion
Tidsramme: within 7 days after delivery
need for blood transfusion due to primary postpartum haemorrhage
within 7 days after delivery
Duration of hospital stay after delivery
Tidsramme: upto 6 weeks postpartum
Number of days of hospital stay after delivery due to primary postpartum haemorrhage
upto 6 weeks postpartum
Number of participants with side effects
Tidsramme: within 7 days after delivery
Including nausea, vomiting, diarrhea, headache, abdominal pain, metallic taste, high blood pressure (defined by persistently high blood pressure >=140/90mmHg), shivering, pyrexia (>38.5C)
within 7 days after delivery
Percentage of maternal infection
Tidsramme: within 7 days after delivery
Positive microbiological cultures in high vaginal swab / endocervical swab / blood culture or clinical infection treated by a course of antibiotics
within 7 days after delivery
Patient satisfaction
Tidsramme: within 7 days of delivery
Patient satisfaction regarding the use of sublingual misoprostol by questionnaire
within 7 days of delivery

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: Diana Man Ka Chan, MBBS, Department of Obstetrics & Gynaecology, Queen Mary Hospital

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Forventet)

1. april 2022

Primær fullføring (Forventet)

1. juni 2024

Studiet fullført (Forventet)

1. juni 2024

Datoer for studieregistrering

Først innsendt

1. juli 2021

Først innsendt som oppfylte QC-kriteriene

1. oktober 2021

Først lagt ut (Faktiske)

15. oktober 2021

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

3. mars 2022

Siste oppdatering sendt inn som oppfylte QC-kriteriene

1. mars 2022

Sist bekreftet

1. mars 2022

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Kliniske studier på Misoprostol

Kliniske studier på Misoprostol

3
Abonnere