NCT02604602

Brief Summary

Objective is to analyze a possible association of coagulation factors peripartal with the occurrence of postpartum hemorrhage.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2015

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2015

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

November 11, 2015

Completed
2 days until next milestone

First Posted

Study publicly available on registry

November 13, 2015

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2018

Completed
1.5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

April 20, 2020

Completed
Last Updated

April 22, 2020

Status Verified

April 1, 2020

Enrollment Period

3.1 years

First QC Date

November 11, 2015

Last Update Submit

April 21, 2020

Conditions

Postpartum Hemorrhage

Keywords

PPH

Outcome Measures

Primary Outcomes (1)

  • occurrence of PPH

    7 days

Study Arms (2)

PPH

Other: blood exam

non-PPH

Other: blood exam

Interventions

blood examOTHER

laboratory test

PPHnon-PPH

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

pregnant women before delivery

You may qualify if:

  • pregnant women \> 22 weeks of gestation

You may not qualify if:

  • age \< 18 years, no informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital of Zurich

Zurich, 8091, Switzerland

Location

MeSH Terms

Conditions

Postpartum Hemorrhage

Condition Hierarchy (Ancestors)

Obstetric Labor ComplicationsPregnancy ComplicationsFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesPuerperal DisordersUterine HemorrhageHemorrhagePathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Christian Haslinger, M.D.

    Division of Obstetrics, University Hospital of Zurich

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
2 Weeks
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 11, 2015

First Posted

November 13, 2015

Study Start

October 1, 2015

Primary Completion

November 1, 2018

Study Completion

April 20, 2020

Last Updated

April 22, 2020

Record last verified: 2020-04

Locations

CH(1)