Intrauterine Stent Placement Following Hysteroscopic Septum Resection

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorWeill Medical College of Cornell University

About this trial

The study hopes to learn the best way to prevent internal scar tissue after septum removal. The use of an intrauterine foley catheter balloon may prevent the formation of adhesions following surgery.

Eligibility criteria

Qualifiers

Age 18 and above

Patients electing to undergo hysteroscopic septoplasty following an informed consent and shared decision making process

Uterine septum of at least 50% of the uterine cavity length as quantified on 3-dimensional saline infusion ultrasound

Disqualifiers

Unwilling or unable to provide informed consent

History of prior uterine septum resection

History of prior transmural uterine surgery

Preexisting intrauterine adhesions or prior treatment for intrauterine adhesions

Trial design

Treatments tested in this trial

  • Intraoperative placement of an inflated intrauterine pediatric foley catheter
  • No Catheter placement
  • Hormonal Therapy Agent
  • Oral antibiotics

Treatment groups

320 Participants
are divided into 2 treatment groups