Endometrial Diseases Clinical Trial
Official title:
Fast Versus Slow Tenaculum Placement for Office Procedures: A Randomized Controlled Trial
Verified date | March 2018 |
Source | University of Iowa |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the study is to investigate whether the speed of tenaculum placement affects perceived patient pain during office transcervical procedures.
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 |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Abbey Hardy-Fairbanks |
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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