Actively Recruiting

Phase Not Applicable
FEMALE
NCT05940233

Comparison of Rate of Complete Abortion Between Letrozole Plus Misoprostol vs Misoprostol Alone

Led by Queen Savang Vadhana Memorial Hospital, Thailand · Updated on 2024-11-06

70

Participants Needed

1

Research Sites

100 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Comparison of rate of complete abortion between Letrozole plus Misoprostol versus Misoprostol alone in first trimester pregnancy

CONDITIONS

Official Title

Comparison of Rate of Complete Abortion Between Letrozole Plus Misoprostol vs Misoprostol Alone

Who Can Participate

FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed early pregnancy loss by transvaginal ultrasound according to ACOG Practice Bulletin 2018
  • Gestational age less than or equal to 14 weeks
  • Cervical opening 1 cm or less with no conceptus passing through
  • Hematocrit level 30 or higher
  • Systolic blood pressure 95 mmHg or higher
  • Able to give informed consent, communicate in Thai, and attend follow-up visits
Not Eligible

You will not qualify if you...

  • Allergy to Letrozole or Misoprostol
  • Use of intrauterine contraceptive device
  • Currently breastfeeding
  • Diagnosed ectopic pregnancy or undiagnosed adnexal mass
  • Severe or recurrent liver disease or liver enzyme levels (AST or ALT) 3 times or more above normal
  • Multiple pregnancy
  • Uterine fibroids involving the endometrium such as submucous myoma
  • History of thromboembolism or current thromboembolism
  • Serum creatinine level 2 or higher

AI-Screening

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Trial Site Locations

Total: 1 location

1

Sutinee Srimahachota

Bangkok, Yannawa, Thailand, 10120

Actively Recruiting

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Research Team

S

Sutinee Srimahachota, M.D.

CONTACT

C

Chuenrutai Yeekian, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

2

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