Abdominal Pain Clinical Trial
— PEPOfficial title:
Utility of Pelvic Examination in the Evaluation of Threatened Abortion
Verified date | May 2017 |
Source | Boston Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is designed to determine whether the pelvic examination (including bimanual and speculum examination) is necessary in patients with first trimester vaginal bleeding/ lower abdominal pain when an intra-uterine pregnancy (IUP) is seen on ultrasound. Patients with the chief complaint of vaginal bleeding or lower abdominal pain less than 16 weeks and positive HCG will be considered for this non-inferiority-designed clinical trial. All patients who present to the BMC Emergency Department (ED) Mon - Fri from 8am to 11pm and have had serum or urine HCG testing and a formal ultrasound by a credentialed emergency physician or radiology technician as part of standard of care will be screened for further eligibility. Those patients with intra-uterine pregnancies < 16 weeks gestation seen on ultrasound and meet inclusion criteria will then be asked to provide informed consent to participate in the study. Randomization will occur after consent has been obtained. Half of the patients will be randomized to receive pelvic examinations and the other half will not. Further care will be determined by the treating attending physician. The primary outcome will be a composite morbidity endpoint at 30 days, including return visits to the ED, emergency surgery, need for transfusion, infection, or other missed source of bleeding/ pain. Secondary outcomes of interest include ED throughput time, and patient satisfaction.
Status | Completed |
Enrollment | 220 |
Est. completion date | January 2016 |
Est. primary completion date | January 2016 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Chief complaint of vaginal bleeding or lower abdominal pain 2. Intra-uterine pregnancy seen on ultrasound 3. Date < 16 weeks by estimated LMP or ultrasound 4. Age >21 5. Ability to provide written informed consent 6. English speaking Exclusion Criteria: 1. Already enrolled in study 2. Morbid Obesity (BMI > 40) 3. Pelvic exam performed prior to ultrasound results 4. Prisoner 5. Follow up cannot be assured 6. Admitted to hospital 7. Large amount of vaginal bleeding (>10 pads in 24 hours or equivalent) 8. Unstable vital signs (SBP<90 or HR>110) 9. Known cervical carcinoma in the past 1 year 10. Clinical suspicion for alternative syndrome that requires pelvic exam (such as severe pain consistent with ovarian torsion) 11. Report or suspicion of penetrating vaginal trauma 12. Suspicion of Active Labor 13. Reported Sexual Assault 14. Current pregnancy by IVF 15. IUD in place 16. Suspicion of heterotopic pregnancy on ultrasound |
Country | Name | City | State |
---|---|---|---|
United States | Boston Medical Center | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Boston Medical Center |
United States,
Brown J, Fleming R, Aristzabel J, Gishta R. Does pelvic exam in the emergency department add useful information? West J Emerg Med. 2011 May;12(2):208-12. — View Citation
Brown T, Herbert ME. Medical myth: Bimanual pelvic examination is a reliable decision aid in the investigation of acute abdominal pain or vaginal bleeding. CJEM. 2003 Mar;5(2):120-2. — View Citation
Hoey R, Allan K. Does speculum examination have a role in assessing bleeding in early pregnancy? Emerg Med J. 2004 Jul;21(4):461-3. — View Citation
Isoardi K. Review article: the use of pelvic examination within the emergency department in the assessment of early pregnancy bleeding. Emerg Med Australas. 2009 Dec;21(6):440-8. doi: 10.1111/j.1742-6723.2009.01227.x. Review. — View Citation
Seymour A, Abebe H, Pavlik D, Sacchetti A. Pelvic examination is unnecessary in pregnant patients with a normal bedside ultrasound. Am J Emerg Med. 2010 Feb;28(2):213-6. doi: 10.1016/j.ajem.2008.10.018. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Composite Morbidity Endpoint | Adverse events include, but are not limited to, return visits to the Emergency Department, need for hospital admission, emergency procedure, transfusion, infection, or identification of other source of symptoms. | 30 Days | |
Secondary | Patient Satisfaction | 24 Hours | ||
Secondary | Throughput Time | 24 Hours |
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