Actively Recruiting
Opioid-Sparing Effects of Nurse-Delivered Hypnosis During Breast Cancer Surgery
Led by M.D. Anderson Cancer Center · Updated on 2026-03-16
225
Participants Needed
1
Research Sites
272 weeks
Total Duration
On this page
Sponsors
M
M.D. Anderson Cancer Center
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
To hypnosedation alone given before and during surgery on reducing opioid use after surgery compared to standard general anesthesia given alone or with hypnosedation.
CONDITIONS
Official Title
Opioid-Sparing Effects of Nurse-Delivered Hypnosis During Breast Cancer Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Men and women
- Age 18 or older
- Scheduled for a unilateral breast surgical procedure, with or without sentinel lymph node dissection
- Able to read, write, and speak English or Spanish
- Able to sign written informed consent and willing to follow protocol requirements
You will not qualify if you...
- Extreme mobility issues preventing study participation
- Major thought disorders such as schizophrenia, uncontrolled bipolar disorder, or PTSD
- History of chronic opioid use
- Current pain level of 2 or above on a 0-10 scale
- Uncontrolled comorbidities such as diabetes or hypertension
- Involvement in plastic surgery for oncoplastic reconstruction
- Received chemotherapy for current breast cancer diagnosis
- Surgery expected to last longer than 3 hours
- Hearing loss that could prevent hypnosedation facilitation
- Known allergy to propofol or other medications used during surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
M D Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
L
Lorenzo Cohen, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
3
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