Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT05254756
Other study ID # IRB #2020--0110
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date March 21, 2022
Est. completion date October 30, 2022

Study information

Verified date November 2023
Source Rocky Vista University, LLC
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomized single-blinded clinical study will compare the typical 2-bladed plastic disposable vaginal speculum to the novel 5-petal Bouquet speculum on level of patient comfort, visibility of the cervix, and time length of the examination. The data will be collected via patient and provider questionnaires.


Description:

For nearly 200 years, the traditional 2-blade "Duck bill" vaginal speculum has had very little evolution in design. In past decades, there has been an increase in popularity in using the plastic speculum rather than the metal speculum. The plastic speculum has effectively the same design as the traditional metal vaginal speculum. The current 2-blade design that has been used for centuries leaves many women feeling pain or discomfort during a speculum vaginal exam. Furthermore, in obese and multiparous women, the 2-blade design often allows the lateral walls of the vagina to cave inward during the exam, preventing the provider from gaining full visibility of the cervix. Another common complaint is that the exam takes too long, which leaves patients in pain and feeling vulnerable for an extended period of time. The novel 5-petal Bouquet vaginal speculum offers an alternative design that some have argued provides enhanced patient comfort, better visualization of the cervix, and is easier to use for the provider. This proposed study design is a blueprint that will be used to compare the Bouquet speculum to a traditional 2-blade disposable plastic speculum on patient comfort, visualization of the cervix, and ease of use for the provider. The investigators predict that the results of this study will help physicians and other medical providers provide patients with better experience, reducing or eliminating the current common complaints regarding how speculum exams are performed today.


Recruitment information / eligibility

Status Terminated
Enrollment 13
Est. completion date October 30, 2022
Est. primary completion date October 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Female patients that require a pelvic exam. - 18 years of age or older - Having had at least one previous pelvic exam with the traditional speculum - Consent to participate in the study Exclusion Criteria: - Never had a pelvic exam before

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Bouquet speculum
Quantitative assessments of visualization of cervix, ease-of-use by the provider, and comfort of the patient
Traditional plastic 2-blade disposable speculum
Quantitative assessments of visualization of cervix, ease-of-use by the provider, and comfort of the patient

Locations

Country Name City State
United States St. George OB/GYN Saint George Utah

Sponsors (1)

Lead Sponsor Collaborator
Isain Zapata

Country where clinical trial is conducted

United States, 

References & Publications (1)

Bouquet JM, Chernau A, McLaughlin R, Choudhury Q. 2019. A New Vaginal Speculum and an Inexpensive Kit to Screen and Treat Dysplasia and Cancer of the Cervix. Journal of Women's Health Care. 8.470 doi: 10.35248/2167-0420.19.8.470

Outcome

Type Measure Description Time frame Safety issue
Primary Patient comfort Find the difference in the level of patient comfort during a vaginal speculum exam between the traditional 2-blade plastic disposable speculum and the 5-petal Bouquet speculum.
Assessed with a questionnaire answered by the patient:
What was the level of comfort with this Pap smear compared to other speculum exams you have had? (More comfortable, Same level of comfort/discomfort, Less comfortable )
Based on what you anticipated the exam was:
(More comfortable, As comfortable/uncomfortable, Less comfortable)
On a scale from 0 to 10, what is the highest level of pain you experienced during the Pap smear/speculum exam? (10 being the worst pain you have ever experienced, and 0 being no pain)
Did the doctor who performed the exam ask you adjust your body position while the speculum was inserted? (Yes, No)
What is your estimation of how long the speculum was inserted? (0-30 seconds, 30-60 seconds, 1-2 minutes, 2-3 minutes, >3 minutes)
Immediately after the exam
Primary Length of time Find the difference in the length of time that the Bouquet speculum is inserted during a Pap smear compared to the traditional 2-blade speculum.
The time the speculum is inserted is recorded for every interactions.
During the exam
Primary Ease of use Find the difference in ease of use for the provider between the traditional 2-blade plastic disposable speculum and the 5-petal Bouquet speculum.
Assessed with a questionnaire answered by the provider:
During the speculum exam, were the lateral walls of the cervix easily visualized upon initial visualization of the cervix? (Yes, No)
What is your estimate of how long the speculum was inserted? (0-30 seconds, 30-60 seconds, 1-2 minutes, 2-3 minutes, >3 minutes)
While the speculum was inserted, was the patient asked to adjust body position in order to gain a better view of the cervix? (Yes, No)
Were special maneuvers performed in order to better visualize the cervix? (e.g. use a different size/type of speculum, apply a condom over the speculum to view the lateral walls, re-insert the speculum, etc.)? (Yes, No)
Immediately after the exam
See also
  Status Clinical Trial Phase
Completed NCT03785548 - Utilization of the Mirror During Pelvic Exams