Clin2
NCT05955768Possibly a fitEnrolling by invitation

Lidocaine in a cervical dilator to reduce removal pain

Cervical Dilatations

Part of Pain, Women’s health & pregnancy clinical trials.

This study tests whether putting lidocaine (a numbing medicine) into a disposable cervical dilator can reduce pain during uterine device removal done with local anesthesia. If you’re eligible, your experience of pain is measured so researchers can compare comfort between study procedures.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
74 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • You are between 18 and 64 years old
  • You are voluntarily requesting removal of an intrauterine device (IUD) with local numbing medicine
  • You have no history of allergy or strong sensitivity to lidocaine, salt water, or the dilator material
  • You are willing and able to take part in the study
  • You do not have known problems that change or distort the uterine cavity (like deformation or compressing fibroids)
  • You do not have untreated cervix inflammation or pelvic infection, and you have not had cervical surgery

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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