Hysteroscopy for the Diagnosis and Treatment of Pregnancy of Unknown Location
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Hysteroscopy for diagnosis and treatment of pregnancy of unknown location.
- Who it may be relevant to
- Registry conditions: Pregnancy of Unknown Location. Basic parameters: from 18 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Infertility patients have a higher baseline risk of ectopic pregnancy compared to the general population. If an early pregnancy is not visible by ultrasound, patients with a pregnancy of unknown location (PUL) will undergo uterine aspiration (D\&C) in order to diagnose an ectopic pregnancy and/or treat an abnormal intrauterine pregnancy destined for miscarriage. If the pathologic specimen obtained after D\&C does not contain chorionic villi, the presumptive diagnosis of ectopic pregnancy is made and methotrexate therapy is typically recommended. In many institutions, a D\&C must be scheduled in the operating room so that it may be performed under anesthesia, potentially delaying the urgent treatment of ectopic pregnancy. Office hysteroscopy is a safe and well-tolerated means of evaluating the uterine cavity, though little literature exists supporting its use in the evaluation of PUL. The objective of this study is to compare hysteroscopic biopsy to the gold standard D\&C for the diagnosis and treatment of PUL. The investigators propose a prospective study including patients undergoing care at the University of Pennsylvania. Patients will be included if they have at least three bHCG values demonstrating a \<50% increase in over 48 hours. A hysteroscopy with possible biopsy followed by uterine aspiration will be performed, and the final pathology results will be compared. Although pathology results from the procedure are considered the gold standard of diagnosis, physicians typically do not wait for results to return before proceeding with necessary treatment. Instead, all patients will have a serum bHCG drawn on post-operative day 1, and those with a \<50% decrease compared to pre-procedural values will undergo treatment with methotrexate therapy per institutional protocol. The findings from this pilot study will inform future research comparing hysteroscopic vs. D\&C for management of PUL. If hysteroscopic targeted biopsy is more accurate than D\&C in detecting an abnormal IUP, this technique could reduce unnecessary methotrexate exposure in patients with abnormal IUPs. If adapted to the office setting, hysteroscopic biopsy could also shorten time to diagnosis and definitive treatment. In addition, targeted treatment in the office setting could lower the rate of intrauterine adhesions, and may improve overall the patient experience.
Interventions
- Diagnostic test Hysteroscopy for diagnosis and treatment of pregnancy of unknown location
All patients in this trial will have a diagnostic hysteroscopy performed prior to a dilation and curettage in the treatment of their pregnancy of unknown location
Primary outcome measures
- Presence or absence of abnormal tissue within the endometrial cavity [Time frame: From enrollment to 1 week post-operatively]
Secondary outcome measures (4)
- Sensitivity of hysteroscopy compared to gold-standard dilation and curettage [Time frame: From enrollment to 1 week post-operatively]
- Specificity of hysteroscopy compared to gold-standard dilation and curettage [Time frame: From enrollment to 1 week post-operatively]
- Positive predictive value of hysteroscopy compared to gold-standard dilation and curettage [Time frame: From enrollment to 1 week post-operatively]
- Negative predictive value of hysteroscopy compared to gold-standard dilation and curettage [Time frame: From enrollment to 1 week post-operatively]
Eligibility criteria
Inclusion criteria
- Patients 18 years of age and older
- Patients undergoing care with (1) positive serum hcg and (2) abnormal hcg trend, as defined by <50% rise in bHCG over 48h period, repeated across three lab values.
- Patients with pregnancy via unassisted conception, conception after ovulation induction and/or intrauterine insemination, and/or embryo transfer
- Well established pregnancy dating, either with known LMP, or dating by IUI or embryo transfer
Exclusion criteria
- Patients with known abnormal cavity (history of fibroids, septum, or uterine anomaly)
- Patients who are hemodynamically unstable or with an acute abdomen
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Diagnostic
Study locations
United States · 1 center
- Penn Fertility Care — Philadelphia
Identifiers
NCT: NCT07469605 · 859064