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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02716636
Other study ID # 201509756
Secondary ID
Status Completed
Phase N/A
First received November 17, 2015
Last updated March 19, 2018
Start date April 11, 2016
Est. completion date March 6, 2017

Study information

Verified date March 2018
Source University of Iowa
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to investigate whether the speed of tenaculum placement affects perceived patient pain during office transcervical procedures.


Description:

IUD insertion and endometrial biopsies are commonly performed in office procedures that use a tenaculum to stabilize the cervix. Patient's often complain that tenaculum placement is one of the most uncomfortable parts of these procedures. Patient's who agree to be in the study will be randomized into one of two groups, either slow tenaculum placement or fast tenaculum placement. Throughout the procedure patient's will be asked to rate the amount of pain they are experiencing using a visual analog scale. The researchers will then compare the two groups. The providers will also rate what they perceived the patient's pain to be with the procedure.


Recruitment information / eligibility

Status Completed
Enrollment 121
Est. completion date March 6, 2017
Est. primary completion date March 6, 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years old and older

- Clinic provider plans a transcervical procedure (IUD placement or endometrial biopsy)

- English speaking and able to consent

Exclusion Criteria:

- Incarcerated

- Prior LEEP (loop electrosurgical excision procedure), cryo (cryotherapy) or CKC (cold knife cone) of the cervix

Study Design


Intervention

Procedure:
Slow placement of the tenaculum
Slow placement of the tenaculum on the cervix

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Abbey Hardy-Fairbanks

Outcome

Type Measure Description Time frame Safety issue
Primary Pain with tenaculum placement assessed using a VAS scale Subjects will record their pain on a paper VAS scale at the time of the procedure only. This is the only data collection point for this measure. procedure
Secondary Overall pain perception assessed using a VAS scale Subjects will record their pain on a paper VAS scale at the time of the procedure only. This is the only data collection point for this measure. procedure
Secondary Provider perception of patient pain assessed using a VAS scale Providers will record their pain on a paper VAS scale at the time of the procedure only. This is the only data collection point for this measure. procedure
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