This study seeks to evaluate pregnancy outcomes following hysteroscopic uterine cavity expansion surgery for patients with dysmorphic uterine cavities and poor reproductive histories. Patients already planning to undergo surgery at the recommendation of their physicians will be recruited for participation.
Any patient scheduled to undergo hysteroscopic expansion of the uterine cavity at RMANJ is eligible to participate in the study. Patients will be approached for consent to participate in the study prior to undergoing surgery. If enrolled, outcomes following surgery will be followed and recorded.
Study Type
OBSERVATIONAL
Enrollment
9
Reproductive Medicine Associates of New Jersey
Basking Ridge, New Jersey, United States
Ongoing pregnancy
presence of a fetal heartbeat at 8 weeks gestation
Time frame: 2 years
Change in endometrial volume
Increase or decrease in endometrial volume post-operatively as assessed by saline sonography
Time frame: 1 month
Time to conceive
Time from post-operative visit to conception
Time frame: 2 years
Chemical pregnancy
Positive pregnancy test
Time frame: 2 years
Clinical pregnancy
Presence of a gestational sac on ultrasound
Time frame: 2 years
Pregnancy loss
Miscarriage; either biochemical or clinical pregnancy loss
Time frame: 2 years
Ectopic pregnancy
Pregnancy outside the uterus
Time frame: 2 years
Live birth
Delivery of a liveborn infant
Time frame: 2 years
Obstetrical complications
Any complications including hypertensive diseases, hemorrhage, etc.
Time frame: 2 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Gestational age at delivery
in weeks and days
Time frame: 2 years
Birthweight
in grams
Time frame: 2 years