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Clinical Trial Summary

There are no universal treatment guidelines available. The ultimate purpose of the management of CSP is to simultaneously remove the pregnancy and successfully preserve the woman's fertility (Gonzalez & Tulandi, 2017). A variety of medical and surgical treatment modalities for CSP have been reported; however, most of these are based on low‐level evidence(Sun et al., 2019).


Clinical Trial Description

This will be a randomized clinical trial to evaluate the effect of administration of methotrexate before surgery in reducing bleeding, injury to bladder and ureter, operative time and removing of CSP mass.This will be in comparison to surgery alone in cases of first trimester cesarean scar pregnancy ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04379219
Study type Interventional
Source Mansoura University
Contact Maher Elesawi Elgaly, M.D MRCOG
Phone +2 01016406182
Email mahereleswi@yahoo.com
Status Recruiting
Phase Phase 4
Start date December 1, 2019
Completion date December 2020

See also
  Status Clinical Trial Phase
Not yet recruiting NCT03218059 - Outcome After MTX & Transvaginal Surgery or UAE & Uterine Curettage in Patients With Cesarean Scar Pregnancy N/A
Completed NCT04955028 - MRI in Predicting Intraoperative Massive Hemorrhage for Cesarean Scar Pregnancy
Completed NCT05839574 - Letrozole add-on in the Treatment of Cesarean Scar Pregnancy N/A