๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-03-21

Methoxyflurane for Analgesia During Hysteroscopy (NCT06899724)

A Randomized Multicentre Placebo Controlled Non-inferiority Study of Intravenous Sedation Versus Methoxyflurane During Hysteroscopy.

๐ŸŸก Not Yet Recruiting Observational / Diagnostic ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Dr. John A. Thiel Medical Professional Corporation

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This study is to assess the non-inferiority of using inhaled methoxyflurane (MOF) versus intravenous conscious sedation with fentanyl and midazolam on women's perception of pain, during hysteroscopy and/or polypectomy in an outpatient setting. The researchers will determine whether the participants receiving the inhaled MOF (experimental group) achieve similar clinical effects in reduction of pain and ability to complete the procedure. Women's perception of pain will be recorded on a scale from 0 to 10 using the numeric rating scale (NRS).

Who can join: Review the eligibility criteria below.

Location: University of Saskatchewan โ€” Saskatoon, Saskatchewan

Age range: 25 Years to 75 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (1 Sites)

  • University of Saskatchewan โ€” Saskatoon, Saskatchewan

๐Ÿ“ž Contact the Study Coordinator

Phone: (306) 591-1773

Email: drjthiel@aol.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Analgesia clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—