Trials / Completed
CompletedNCT05198141
Evaluation of Different Doses of Letrozole in Ectopic Pregnancy
Evaluation of Different Doses of Aromatase Inhibitor Letrozole for the Treatment of Ectopic Pregnancy
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Zagazig University · Other Government
- Sex
- Female
- Age
- 19 Years – 35 Years
- Healthy volunteers
- Not accepted
Summary
The utilization of letrozole at a daily dose of 10 mg for medical treatment of ectopic pregnancy considerably has a high success rate without imposing any serious side effects compared to daily 5mg letrozole.
Detailed description
Letrozole, an aromatase inhibitor, has recently been introduced as favorable medical treatment for ectopic pregnancy. We aimed at evaluating the effects of different doses of letrozole for induction of abortion Sixty patients with undisturbed ectopic pregnancy were classified into three equal groups. Group I: The control group that contained women who were undergoing laparoscopic salpingectomy, Group II: Patients who received letrozole (5 mg d-1) for 10 d, and Group III: Patients who received letrozole (10 mg d-1) for 10 d. After that, the human chorionic gonadotropin (β-hCG) levels were determined for the first day and after 11 d of treating. letrozole (10 mg d-1) markedly reduced the receptors of estrogen and progesterone, and subsequent vascular endothelial growth factor signals, resulting in marked apoptosis in the placenta tissue. The utilization of letrozole at a dose of 10 mg d-1 for inducement of abortion typically results in a substantial high-successful rate without any severe side effects.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Letrozole tablets | GI: Patients who were undergoing laparoscopic salpingectomy GII: patients who medically treated with 5 mg d-1 of letrozole using two tablets (2.5 mg of Femara) every day for 10 d GIII patients who medically treated with 10 mg d-1 of letrozole using four tablets (2.5 mg of Femara) every day for 10 d (group III) |
| PROCEDURE | laparoscopic salpingectomy | laparoscopic salpingectomy |
Timeline
- Start date
- 2020-12-15
- Primary completion
- 2021-11-20
- Completion
- 2022-01-01
- First posted
- 2022-01-20
- Last updated
- 2022-01-20
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT05198141. Inclusion in this directory is not an endorsement.