MedPath

Novel Cervical Retraction Device

Not Applicable
Conditions
Pain Due to Certain Specified Procedures
Interventions
Device: Intrauterine device (IUD) insertion
Procedure: Endometrial biopsy
Registration Number
NCT02283463
Lead Sponsor
Bioceptive
Brief Summary

This study will test a suction-based method of engaging the cervix. Bioceptive has developed a device that more gently and atraumatically attaches to the cervix with no bleeding. This novel attachment mechanism may diminish pain and discomfort. Pre-clinical testing has been performed on the device including testing on synthetic uterine models, human cadavers, and human uteri immediately post-hysterectomy (Utah IRB # 00059096). Results from these efforts have shown effective attachment to the cervix and the ability for the device to maintain suction throughout a procedure atraumatically. This study proposes to introduce this minimal risk device in a clinical setting to determine the response of women undergoing gynecologic procedures.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
24
Inclusion Criteria
  • Subjects presenting for IUD insertion or endometrial biopsy
  • Able to consent for study in English or Spanish
Exclusion Criteria
  • Post-menopausal
  • Current pregnancy
  • Cervical abnormalities (cervical polyp, cervical lesion, or irregularity)
  • Use of narcotics or Benzodiazepines prior to procedure

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Standard Cervical TenaculumEndometrial biopsySingle tooth tenaculum, pierces the tissue of the cervix to allow provider to stabilize and place traction on the cervical cal/uterus
Standard Cervical TenaculumIntrauterine device (IUD) insertionSingle tooth tenaculum, pierces the tissue of the cervix to allow provider to stabilize and place traction on the cervical cal/uterus
Bioceptive Cervical Retraction DeviceIntrauterine device (IUD) insertionSuction based method for stabilizing the cervix and uterus. Achieves suction 360 degrees around cervical os creating a portal through which instruments can be passed into the cervical canal and uterus. Provider can still place traction on uterus with this device just as with tenaculum.
Bioceptive Cervical Retraction DeviceEndometrial biopsySuction based method for stabilizing the cervix and uterus. Achieves suction 360 degrees around cervical os creating a portal through which instruments can be passed into the cervical canal and uterus. Provider can still place traction on uterus with this device just as with tenaculum.
Primary Outcome Measures
NameTimeMethod
Pain Intensity Measure 100 point visual analogue scale1 day

Pain recorded by patient during the procedure and one day following via 100 point visual analogue scale. (0 = none, 100 = worst imaginable)

Secondary Outcome Measures
NameTimeMethod
Procedural Satisfaction Patient records level of satisfaction with the procedure (Very Unsatisfied, Unsatisfied, Neutral, Satisfied, Very Satisfied)< 1 hour

Patient records level of satisfaction with the procedure (Very Unsatisfied, Unsatisfied, Neutral, Satisfied, Very Satisfied)

Trial Locations

Locations (1)

University of Utah, School of Medicine

🇺🇸

Salt Lake City, Utah, United States

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