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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05198050
Other study ID # Letrozole and abortion
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 3, 2022
Est. completion date September 30, 2022

Study information

Verified date September 2023
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Some studies suggest the prescription of aromatase inhibitors prior to the use of misoprostol for inducing drug abortion. the aim of the study is to compare the effectiveness of various regimens of letrozole combined with misoprostol versus using misoprostol alone in inducing complete abortion in patients with blighted ovum.


Description:

Some studies suggest prescription of aromatase inhibitors prior to the use of misoprostol for inducing drug abortion, increases the efficiency of the treatment regimen and also decreases the need for surgical interventions. Some conducted studies have mentioned reinforcing the impact of misoprostol with letrozole, but reaching the ideal dose still needs more studies, so in this study, the investigators will compare the effectiveness of various regimens of letrozole ( 10 mg/d for 3 days or a single dose of 20 mg) combined with misoprostol versus using misoprostol alone in inducing complete abortion in patients with a blighted ovum.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date September 30, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - first trimester of pregnancy - pregnancy duration less than 12 weeks based on LMP. - non-viable fetus (blighted ovum) Exclusion Criteria: - No heart disease, - No asthma - No History of thromboembolism - No History of cancer - No renal failure - No liver diseases - History of allergy to misoprostol or letrozole drugs.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Letrozole tablets
Letrozole is a third-generation non-steroidal aromatase inhibitor
Misoprostol Tabets
a synthetic prostaglandin medication
Placebo tablets
Placebo tables with a similar appearance to letrozole

Locations

Country Name City State
Egypt Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

References & Publications (4)

Abbasalizadeh F, Sahhaf F, Sadeghi-Shabestari P, Mirza-Aghazadeh-Attari M, Naghavi-Behzad M. Comparison Between Effect of Letrozole Plus Misoprostol and Misoprostol Alone in Terminating Non-Viable First Trimester Pregnancies: A Single Blind Randomized Trial. J Family Reprod Health. 2018 Mar;12(1):27-33. — View Citation

Fouda UM, Sayed AM. Extended letrozole regimen versus clomiphene citrate for superovulation in patients with unexplained infertility undergoing intrauterine insemination: a randomized controlled trial. Reprod Biol Endocrinol. 2011 Jun 21;9:84. doi: 10.1186/1477-7827-9-84. — View Citation

Lee VC, Yeung TW, Tang OS, Ng EH, Yeung WS, Ho PC. Effect of letrozole on uterine artery Doppler flow indices prior to first-trimester termination of pregnancy: a randomized controlled trial. Ultrasound Obstet Gynecol. 2012 Oct;40(4):392-7. doi: 10.1002/uog.11115. — View Citation

Lee VCY, Ng EHY, Yeung WSB, Ho PC. Misoprostol with or without letrozole pretreatment for termination of pregnancy: a randomized controlled trial. Obstet Gynecol. 2011 Feb;117(2 Pt 1):317-323. doi: 10.1097/AOG.0b013e3182073fbf. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Complete abortion no emergency or elective curettage was necessary until next menstruation 2 days
Secondary Induction-to-abortion interval the interval between administration of misoprostol) 2 days
Secondary Adverse effects of Misoprostol diarrhea, abdominal cramps, fever and sweating. 2 days
Secondary Adverse effects of Letrozole hot flushes, drowsiness and nausea. 2 days
See also
  Status Clinical Trial Phase
Completed NCT05216952 - Ulipristal Acetate for Use in Early Pregnancy Loss Phase 2
Completed NCT00177372 - Mifepristone and Misoprostol for Fetal Demise Phase 4
Terminated NCT00468299 - MiMi: A Randomized Trial of Mifepristone and Misoprostol for Treatment of Early Pregnancy Failure N/A