Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06554470

Local vs Systemic Methotrexate in Management of Uterine Ectopic Pregnancy

Local Versus Systemic Methotrexate in Management of Uterine Ectopic Pregnancy: A Randomized Trial

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
34 (estimated)
Sponsor
Tanta University · Academic / Other
Sex
Female
Age
20 Years – 40 Years
Healthy volunteers
Not accepted

Summary

This study aims to compare local and systemic methotrexate in the management of uterine ectopic pregnancy regarding the duration of beta human chorionic gonadotropin (hCG) clearance and need for further management options.

Detailed description

Ectopic pregnancy is considered a life-threatening condition which requires immediate intervention. Owing to the advancements in medical technology, ectopic pregnancy can now be diagnosed in the early stages. Methotrexate (MTX) is an antimetabolite drug showing a competitive reversible binding concerning natural dihydrofolates and acting as an inhibitor of the dihydrofolate-reductase (DHFR), a key enzyme synthesizing the tetrahydrofolates needed for the synthesis of purine and pyrimidine rings.

Conditions

Interventions

TypeNameDescription
DRUGSystemic MethotrexatePatients will receive systemic methotrexate (intramuscular; 50 mg/m2 body weight).
DRUGLocal MethotrexatePatients will receive local methotrexate (25 mg methotrexate as a fixed dose).

Timeline

Start date
2024-08-15
Primary completion
2025-07-01
Completion
2025-07-01
First posted
2024-08-15
Last updated
2024-08-16

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06554470. Inclusion in this directory is not an endorsement.