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Study identifier: NCT07157423 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Research Study to See How Safe is Eptacog Alfa When Used to Stop Heavy Bleeding in Women After Giving Birth in India

Condition: Severe Postpartum Haemorrhage  ·  Sponsor: Novo Nordisk A/S

PhasePhase 4
Planned participants64
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study will look at how safe is the medicine eptacog alfa when used in women in India for stopping heavy bleeding after giving birth. If participants have heavy bleeding after giving birth then they will get the medicine eptacog alfa. This study will be conducted to get more knowledge on the safety of the medicine eptacog alfa use in these women. At first participants will receive one dose of medicine eptacog alfa. If the given dose is not helpful to stop the bleeding, participants will get one additional dose. The study will last for about 30-35 days.

This description comes directly from the study's public registry record.

Talk to the study team

Novo Nordisk  ·  (+1) 866-867-7178  ·  clinicaltrials@novonordisk.com

Always discuss trial participation with your own doctor first.

Locations (10)

KLE BelgumBelagavi, Karnataka, IndiaRecruiting
Calicut Medical CollegeKozhikode, Kerala, IndiaRecruiting
Calicut Medical CollegeKozhikode, Kerala, IndiaNot Yet Recruiting
Seth GS Medical College & KEM HospitalMumbai, Maharashtra, IndiaRecruiting
All India Institute of Medical Sciences_New DehliNew Delhi, National Capital Territory of Delhi, IndiaRecruiting
SMS HospitalJaipur, Rajasthan, IndiaRecruiting
SMS HospitalJaipur, Rajasthan, IndiaNot Yet Recruiting
KLE BelgumBelagavi, IndiaNot Yet Recruiting
Post Graduate Institute of Medical Education & Research_ChandigarhChandigarh, IndiaRecruiting
Post Graduate Institute of Medical Education & Research_ChandigarhChandigarh, IndiaNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07157423