Clin2
NCT06640738Possibly a fitNot yet recruiting

Best sedation dose for uterine fibroid ablation

Uterine Fibroids (UF)

Part of Cancer clinical trials.

This study tests two different levels of sedation medicines (Remifentanil and Dexmedetomidine) to find the best dose for women undergoing a procedure to shrink uterine fibroids. The goal is to make the procedure more comfortable and safe.

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

Phase
Phase 4
Enrollment
60 people
Ages
20 years to 65 years
Study type
Interventional

Who can take part

  • You are between 20 and 65 years old
  • You have been diagnosed with uterine fibroids
  • You do not have serious heart disease, kidney disease, or liver problems
  • You are not allergic to the drug Remifentanil
  • You are willing to join the study

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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