Hysteroscopy for the Diagnosis and Treatment of Pregnancy of Unknown Location

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of Pennsylvania

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Patients with known abnormal cavity (history of fibroids, septum, or uterine anomaly)

Patients who are hemodynamically unstable or with an acute abdomen

Trial design

Design model

Single group

Treatments tested in this trial

  • Hysteroscopy for diagnosis and treatment of pregnancy of unknown location

    Diagnostic test

    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

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Hysteroscopy prior to Dilation and CurettageExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Presence or absence of abnormal tissue within the endometrial cavity

Intra-operative photographs will be taken of the participants uterine cavities at five standardized locations (left cornua, right cornua, anterior uterine wall, posterior uterine wall, and entire uterine cavity at level of internal os). The presence or absence of abnormal tissue will be documented, and findings qualitatively compared between the cavities of participants with the final diagnosis of non-viable intrauterine pregnancy and an ectopic pregnancy.

Time frame
From enrollment to 1 week post-operatively

Secondary outcomes

1

Sensitivity of hysteroscopy compared to gold-standard dilation and curettage

Sensitivity, specificity, and positive and negative predictive values of hysteroscopic biopsy as a diagnostic test will be compared to that of D\&C. Statistical significance will be determined with the use of Fisher exact test analysis with Stata software, with a probability value of \<0.05 considered statistically significant

Time frame
From enrollment to 1 week post-operatively
2

Specificity of hysteroscopy compared to gold-standard dilation and curettage

Specificity of hysteroscopic biopsy as a diagnostic test will be compared to that of D\&C. Statistical significance will be determined with the use of Fisher exact test analysis with Stata software, with a probability value of \<0.05 considered statistically significant

Time frame
From enrollment to 1 week post-operatively
3

Positive predictive value of hysteroscopy compared to gold-standard dilation and curettage

Positive predictive value of hysteroscopic biopsy as a diagnostic test will be compared to that of D\&C. Statistical significance will be determined with the use of Fisher exact test analysis with Stata software, with a probability value of \<0.05 considered statistically significant

Time frame
From enrollment to 1 week post-operatively
4

Negative predictive value of hysteroscopy compared to gold-standard dilation and curettage

Negative predictive value of hysteroscopic biopsy as a diagnostic test will be compared to that of D\&C. Statistical significance will be determined with the use of Fisher exact test analysis with Stata software, with a probability value of \<0.05 considered statistically significant

Time frame
From enrollment to 1 week post-operatively

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Pennsylvania

Lead sponsor

American Society for Reproductive Medicine

Collaborator