Clin2
NCT07458295Possibly a fitRecruiting

Liposomal bupivacaine for pain after gynecologic cancer surgery

Laparoscopic SurgeryGynecologic Oncology PatientLiposomal BupivacaineTransversus Abdominis Plane Block

Treatments studied

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

This trial tests whether a long-acting numbing medication (liposomal bupivacaine) injected into the abdominal wall can reduce pain after laparoscopic surgery for gynecologic cancer. If effective, it may help patients recover with less discomfort and fewer painkillers.

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

Phase
N/A
Enrollment
110 people
Ages
18 years to 64 years
Study type
Interventional

Who can take part

  • You are scheduled for laparoscopic surgery for gynecologic cancer (not emergency surgery).
  • You are between 18 and 64 years old.
  • You are in generally good health (ASA class I, II, or III — your anesthesiologist can determine this).
  • You are fully awake and alert (Glasgow Coma Scale score of 15).
  • You do not have any of the following: chronic pain, heart block, unstable heart disease, stomach ulcer or bleeding, diabetes requiring insulin, bleeding disorders, severe liver or kidney problems, a history of mental illness or current psychiatric medication, alcohol or drug abuse, chronic opioid use, pregnancy or breastfeeding, extreme weight (BMI under 15 or over 35), or allergy to the study drugs.

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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