Effect of Prednisolone Treatment on Uterine Natural Killer Cells

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexFemale
Age18-40
SponsorChinese University of Hong Kong

About this trial

This study aims to investigate the role of uNK cells and the association with prednisolone.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Women with a history of 3 or more consecutive miscarriages

Women younger than 40 years old

Disqualifiers

Allergy to prednisolone

Women who have any uterine anomaly

Antiphospholipid syndrome

Hydrosalpinx

Trial design

Design model

Single group

Treatments tested in this trial

  • Prednisolone

    Drug

    prednisolone oral 10 mg/day from day one of the subsequent menstrual cycle to day LH 7 of that cycle. Then, the participants will be given a tailing off dose of 5 mg/day for 3 days followed by 2 mg/day for 3 days and then 1 mg/day for 3 days.

Treatment groups

84 Participants
are divided into 1 treatment group
Group A: prednisoloneExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

the number of uNK cells

to investigate the association between uNK cells and prednisolone

Time frame
at the 1 day of endometrial biopsy

Secondary outcomes

Other outcomes

Sponsors and contacts

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