Active Management of the Third Stage of Labour: Uterine Tonus Assessment by Midwife vs. Patient Self-administration (UTAMP)
Primary Purpose
Postpartum Hemorrhage
Status
Completed
Phase
Not Applicable
Locations
Ghana
Study Type
Interventional
Intervention
Uterine Tonus Assessment by Midwife
Patient self-assessment of uterine tonus
Sponsored by
About this trial
This is an interventional prevention trial for Postpartum Hemorrhage focused on measuring Postpartum hemorrhage, Uterine tonus assessment, Active management of third stage of labor
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years
- Be in labor with an expected vaginal delivery, as assessed by the midwives
- Gestation age ≥ 37 weeks
- Received antenatal instructions on postnatal uterine tonus assessment
- Provided informed consent.
Exclusion Criteria:
- Age <18
- Elective caesarean delivery
- Severe anemia (<8g/dL)
- Placenta praevia
- Anticipated breech delivery
- Referred patients who have not received antenatal care (ANC) uterine tonus assessment instructions
- Multiple Pregnancy
- Intra uterine fetal death
Sites / Locations
- Korle Bu Teaching Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Self-assessment of uterine tonus
Midwife uterine tonus assessment
Arm Description
Uterine tonus assessment every 15 minutes for 2 hours by educated patient, which is standard-of-care.
Uterine tonus assessment every 15 minutes for 2 hours by midwive.
Outcomes
Primary Outcome Measures
Postpartum hemorrhage (>500 ml blood loss)
To determine whether there is a difference in effectiveness of routine uterine tonus assessment (every 15 minutes, for 2 hours) to prevent post-partum hemorrhage (≥500 ml blood loss) when performed by a midwife and self-administered by a patient.
Secondary Outcome Measures
Mean blood loss (in ml)
Severe post-partum hemorrhage
>1000ml blood loss
Use of additional uterotonics
Use of other procedures for management of postpartum hemorrhage
I.e. surgery, manual placenta tissue removal
Late postpartum hemorrhage
Based on readmission
Full Information
NCT ID
NCT02223806
First Posted
August 11, 2014
Last Updated
November 23, 2016
Sponsor
UMC Utrecht
Collaborators
Korle-Bu Teaching Hospital, Accra, Ghana, University of Ghana
1. Study Identification
Unique Protocol Identification Number
NCT02223806
Brief Title
Active Management of the Third Stage of Labour: Uterine Tonus Assessment by Midwife vs. Patient Self-administration
Acronym
UTAMP
Official Title
Active Management of the Third Stage of Labour: Uterine Tonus Assessment by Midwife vs. Patient Self-administration
Study Type
Interventional
2. Study Status
Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
April 2014 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
August 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UMC Utrecht
Collaborators
Korle-Bu Teaching Hospital, Accra, Ghana, University of Ghana
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
To determine whether there is a difference in effectiveness of routine uterine tonus assessment (every 15 minutes, for 2 hours) when performed by a midwife or self-administered by a patient on the incidence of postpartum haemorrhage, mean blood loss, and other maternal and neonatal outcomes.
Detailed Description
Rationale: Postpartum haemorrhage (PPH) is the most common cause of maternal death worldwide. The active management of the third stage of labour (AMTSL) is recognized as an effective strategy to prevent morbidity and mortality associated with PPH and reduce blood loss. AMTSL includes the provision of uterotonic drugs, controlled cord traction, delayed cord clamping and cutting, massage of the uterus, and monitoring of the uterine tonus. Although professional guidelines recommend the steps of AMTSL to be performed by health professionals, the reality of health professionals understaffed hospitals in many low- and middle income countries (LMICs) necessitates task-shifting of the final AMTSL component to patients. Yet, whether uterine tonus assessment yields the same effect when performed by patients and midwives has not been formally evaluated.
Objective: To determine whether there is a difference in effectiveness of routine uterine tonus assessment (every 15 minutes, for 2 hours) when performed by a midwife or self-administered by a patient on the incidence of postpartum haemorrhage . mean blood loss, and other maternal and neonatal outcomes.
Study design: Randomized intervention study. Study population: Pregnant women admitted in the labour to the Korle Bu Teaching Hospital, Accra, Ghana Intervention: the intervention group will receive uterine tonus assessment every 15 minutes for 2 hours by a midwife, the control group will continue the current practice of self-assessment after patient education with regular monitoring of midwives.
Main study parameters/endpoints: post-partum haemorrhage (>500 ml blood loss), severe postpartum haemorrhage (>1000 ml blood loss), mean blood loss, other maternal and neonatal outcomes.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients will receive the standard of midwifery and obstetric care, and will have access to emergency obstetric interventions. All steps of the AMTSL will be performed, with the exemption of the last step of uterine tonus assessment for which women will be randomized to receive the intervention or current practice of care. Risk associated with the intervention are discomfort because of an external assessment. Data will be obtained from record books at the ward. Women will be asked for informed consent prior to participation. This study will be approved by the Ethical en Protocol Review Committee of the University of Ghana Medical School and the Medical Ethical Research Committee of the University Medical Center Utrecht.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postpartum Hemorrhage
Keywords
Postpartum hemorrhage, Uterine tonus assessment, Active management of third stage of labor
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
800 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Self-assessment of uterine tonus
Arm Type
Active Comparator
Arm Description
Uterine tonus assessment every 15 minutes for 2 hours by educated patient, which is standard-of-care.
Arm Title
Midwife uterine tonus assessment
Arm Type
Experimental
Arm Description
Uterine tonus assessment every 15 minutes for 2 hours by midwive.
Intervention Type
Behavioral
Intervention Name(s)
Uterine Tonus Assessment by Midwife
Intervention Description
Uterine tonus assessment every 15 minutes for 2 hours.
Intervention Type
Behavioral
Intervention Name(s)
Patient self-assessment of uterine tonus
Intervention Description
Uterine tonus assessment by patient every 15 minutes for 2 hours.
Primary Outcome Measure Information:
Title
Postpartum hemorrhage (>500 ml blood loss)
Description
To determine whether there is a difference in effectiveness of routine uterine tonus assessment (every 15 minutes, for 2 hours) to prevent post-partum hemorrhage (≥500 ml blood loss) when performed by a midwife and self-administered by a patient.
Time Frame
within 24 hours postpartum
Secondary Outcome Measure Information:
Title
Mean blood loss (in ml)
Time Frame
Within 24 hours postpartum
Title
Severe post-partum hemorrhage
Description
>1000ml blood loss
Time Frame
Within 24 hours postpartum
Title
Use of additional uterotonics
Time Frame
Within 24 hours postpartum
Title
Use of other procedures for management of postpartum hemorrhage
Description
I.e. surgery, manual placenta tissue removal
Time Frame
Within 24 hours postpartum
Title
Late postpartum hemorrhage
Description
Based on readmission
Time Frame
From 24 hours and upto one week
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18 years
Be in labor with an expected vaginal delivery, as assessed by the midwives
Gestation age ≥ 37 weeks
Received antenatal instructions on postnatal uterine tonus assessment
Provided informed consent.
Exclusion Criteria:
Age <18
Elective caesarean delivery
Severe anemia (<8g/dL)
Placenta praevia
Anticipated breech delivery
Referred patients who have not received antenatal care (ANC) uterine tonus assessment instructions
Multiple Pregnancy
Intra uterine fetal death
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joyce L Browne, MD, MSc
Organizational Affiliation
UMC Utrecht, the Netherlands
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kerstin D Klipstein-Grobusch, PhD MSc
Organizational Affiliation
University Medical Center Utrecht, The Netherlands
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nelson Damale, MBChB
Organizational Affiliation
Korle-Bu Teaching Hospital, Accra, Ghana
Official's Role
Principal Investigator
Facility Information:
Facility Name
Korle Bu Teaching Hospital
City
Accra
Country
Ghana
12. IPD Sharing Statement
Citations:
PubMed Identifier
26683621
Citation
Browne JL, Damale NK, Raams TM, Van der Linden EL, Maya ET, Doe R, Rijken MJ, Adanu R, Grobbee DE, Franx A, Klipstein-Grobusch K. Uterine Tonus Assessment by Midwives versus Patient self-assessment in the active management of the third stage of labor (UTAMP): study protocol for a randomized controlled trial. Trials. 2015 Dec 18;16:580. doi: 10.1186/s13063-015-1111-5.
Results Reference
derived
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Active Management of the Third Stage of Labour: Uterine Tonus Assessment by Midwife vs. Patient Self-administration
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