Using hypnosis to reduce opioid use during breast cancer surgery
Opioid-Sparing Effects of Nurse-Delivered Hypnosis During Breast Cancer Surgery
This study is looking at how using hypnosis by nurses during breast cancer surgery can help patients feel less anxious and in less pain, which might mean they need fewer strong pain medications and recover better.
Quick facts
| Grant type | R01 grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | University of Tx Md Anderson Can Ctr NIH-funded |
| Lab location | 1 site (Houston, United States) |
| Project ID | NIH-11085166 on NIH RePORTER |
What this research studies
This research investigates the effects of nurse-delivered hypnosis on patients undergoing breast cancer surgery. By utilizing hypnosedation, the study aims to reduce the need for opioids and general anesthesia, which can lead to various side effects and complications. Patients will receive hypnosis during their surgical procedures to help manage anxiety and pain, potentially leading to improved recovery outcomes and reduced medication use. The approach is based on previous findings that suggest hypnosis can enhance patient comfort and satisfaction.
Who could benefit from this research
Good fit: Ideal candidates for this research are women scheduled for breast cancer surgery who are seeking alternatives to traditional pain management methods.
Not a fit: Patients who are not undergoing breast cancer surgery or those who have contraindications for hypnosis may not benefit from this research.
Why it matters
Potential benefit: If successful, this research could lead to safer surgical experiences for breast cancer patients by minimizing opioid use and its associated side effects.
How similar studies have performed: Previous studies have shown success with hypnosis in various medical procedures, indicating a promising potential for this approach in breast cancer surgery.
Where this research is happening
Houston, United States
- University of Tx Md Anderson Can Ctr — Houston, United States (Active)
Researchers
- Principal investigator: Cohen, Lorenzo — University of Tx Md Anderson Can Ctr
- Study coordinator: Cohen, Lorenzo
About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page below.