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Sufentanil Infusion vs Intravenous Methadone for Postoperative Analgesia Following Head and Neck Dissection With Free Flap or Rotational Reconstruction

StatusRecruiting
PhasePhase 4
Started2025-01-10
View on ClinicalTrials.gov ↗

Amendment history

2026-04-27
Study Status, Sponsor/Collaborators v4
Re-verified, no change to tracked fields
2025-03-28
Study Identification, Study Status, Study Description, Eligibility, Contacts/Locations v3
Eligibility criteria+14 characters
Inclusion Criteria: • Patients undergoing head and neck dissection with free flap or rotational reconstruction at Indiana University Health Adult Academic H [...]
Study sitescontacts updated at 1 of 1 site
Study title+14 characters
Sufentanil Infusion Vsvs Intravenous Methadone for Postoperative Analgesia Following Head and Neck Dissection withWith Free Flap or Rotational Reconstruction
2025-02-11
Study Identification, Study Status, Contacts/Locations v2
Completion date2028-11-04→2027-11-04
Study sitescontacts updated at 1 of 1 site
Study titlerevised
Sufentanil Infusion vsVs Intravenous Methadone for Postoperative Analgesia Following Head and Neck Dissection Withwith Free Flap Reconstruction
2025-01-21
Study Identification, Study Status, Contacts/Locations v1
Study sitescontacts updated at 1 of 1 site
Study title-39 characters
Randomized Prospective Study Comparing Sufentanil Infusion Vsvs Intravenous Methadone for Postoperative Analgesia Following Head and Neck Dissection withWith Free Flap Reconstruction
2025-01-15
Original filing
The main purpose of this study is to determine which type of medication, sufentanil or methadone, is better at controlling pain during and, more importantly, after surgery in patients undergoing a head and neck dissection with free flap or rotational tissue reconstruction. Prior to their operation, subjects will be randomized to receive either Sufentanil or Methadone. After surgery, research staff will obtain information about recovery and pain levels.
Trial Details
NCT Number NCT06784999
Lead Sponsor Indiana University
Conditions Free Flap Reconstruction
Enrollment 128 participants
Start Date 2025-01-10
Primary Completion 2027-11-04 (estimated)
Study Completion 2027-11-04 (estimated)
Updated on ClinicalTrials.gov 2026-05-01